CERTIFICATE. No. P Order No Page 1/2

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1 CERTIFICATE No. P Order No Page 1/2 Product Applicant Manufacturer Factory Ratings Medical power supply for building-in Bel Fuse Inc. 206 Van Vorst St. Jersey City, NJ USA Bel Fuse Inc. 206 Van Vorst St. Jersey City, NJ USA EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez, Andheri (East) Mumbai India See next page(s) AC Input: 3.0A Max, V~, 47-63Hz Trade mark Model / Type Ref. Principal characteristics MBC120-1XXXL-YYY-W Cl. I, Output: Refer to General Product Information Where "X" and "Y" = 0-9, A-Z, a-z or blank, W is blank for Class I See next page(s) A sample of the product was tested and found to be in conformity with MED EN :2006;A11;A1;A12 Validity Additional information This certificate documents conformity with the standards shown, and also applies as license for use of Nemkos name and certification mark. The certificate and license is valid as long as the applicable conditions are complied with, and provided that any changes to the product are notified to Nemko for acceptance prior to implementation. New standards or amendments to the standards may imply that the product design must be updated and/or that re-testing and re-certification is necessary. See next page(s) The abovementioned certified equipment complies with current regulatory requirements regarding electrical safety in Norway and other EU/EEA member states, as far as this can be checked. Compliance with requirements regarding building-in, protection against electric shock and Electromagnetic Compatibility (EMC) must be checked when the equipment is built-in a completed product or forms a part of a complete system. Additional model(s) See next page(s) Date of issue Okhyun Jeon Certification Department Nemko AS Gaustadalléen 30, P.O. Box 73 Blindern, 0314 Oslo, Norway TEL FAX info@nemko.com ENTERPRISE NUMBER NO nemko.com

2 CERTIFICATE No. P Order No Page 2/2 Product Medical power supply for building-in Pos. No 1 Model / Type Ref. MBC75-1XXXL-YYY-W Trade mark (if different from page 1) Rating Principal characteristics AC Input: 2.0A Max, V~ 47-63Hz Cl. I, Output: Refer to General Product Information Where "X" and "Y" = 0-9, A-Z, a-z or blank, W is blank for Class I Date of issue Okhyun Jeon Certification Department Nemko AS Gaustadalléen 30, P.O. Box 73 Blindern, 0314 Oslo, Norway TEL FAX info@nemko.com ENTERPRISE NUMBER NO nemko.com

3 CERTIFICATE No. P Order No Page 1/2 Product Applicant Manufacturer Factory Ratings Medical Power Supply (for building-in) Bel Fuse Inc. 206 Van Vorst St. Jersey City, NJ USA Bel Fuse Inc. 206 Van Vorst St. Jersey City, NJ USA EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez, Andheri (East) Mumbai India See next page(s) AC Input: 3.0A Max, V~ 47-63Hz Trade mark Model / Type Ref. Principal characteristics MBC120-1XXXL-YYY-2 Cl. II. Output rating see the test report. The "X" and "Y" = 0-9, A-Z, a-z or blank See next page(s) A sample of the product was tested and found to be in conformity with MED EN :2006;A11;A1;A12 Validity Additional information This certificate documents conformity with the standards shown, and also applies as license for use of Nemkos name and certification mark. The certificate and license is valid as long as the applicable conditions are complied with, and provided that any changes to the product are notified to Nemko for acceptance prior to implementation. New standards or amendments to the standards may imply that the product design must be updated and/or that re-testing and re-certification is necessary. See next page(s) The abovementioned certified equipment complies with current regulatory requirements regarding electrical safety in Norway and other EU/EEA member states, as far as this can be checked. Compliance with requirements regarding building-in, protection against electric shock and Electromagnetic Compatibility (EMC) must be checked when the equipment is built-in a completed product or forms a part of a complete system. Additional model(s) See next page(s) Date of issue Juan Z. Kleppenes Certification Department Nemko AS Gaustadalléen 30, P.O. Box 73 Blindern, 0314 Oslo, Norway TEL FAX info@nemko.com ENTERPRISE NUMBER NO nemko.com

4 CERTIFICATE No. P Order No Page 2/2 Product Medical Power Supply (for building-in) Pos. No 1 Model / Type Ref. MBC75-1XXXL-YYY-2 Trade mark (if different from page 1) Rating Principal characteristics AC Input: 2.0A Max, V~ 47-63Hz Cl. II. Output rating see the test report. The "X" and "Y" = 0-9, A-Z, a-z or blank Date of issue Juan Z. Kleppenes Certification Department Nemko AS Gaustadalléen 30, P.O. Box 73 Blindern, 0314 Oslo, Norway TEL FAX info@nemko.com ENTERPRISE NUMBER NO nemko.com

5 Ref. Certif. No. NO89049 IEC SYSTEM FOR MUTUAL RECOGNITION OF TEST CERTIFICATES FOR ELECTRICAL EQUIPMENT (IECEE) CB SCHEME SYSTEME CEI DACCEPTATION MUTUELLE DE CERTIFICATS DESSAIS DES EQUIPEMENTS ELECTRIQUES (IECEE) METHODE OC CB TEST CERTIFICATE CERTIFICAT D'ESSAI OC Product Produit Name and address of the applicant Nom et adresse du demandeur Name and address of the manufacturer Nom et adresse du fabricant Name and address of the factory Nom et adresse de l'usine Note: When more than one factory, please report on page 2 Note: Lorsque il y plus d'une usine, veuillez utiliser la deuxième page Ratings and principal characteristics Valeurs nominales et caractéristiques principales Trademark (if any) Marque de fabrique (si elle existe) Medical power supply for ( building-in ) EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez Andheri (East), Mumbai India EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez Andheri (East), Mumbai India EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez Andheri (East), Mumbai India Additional information on page 2 AC Input: 3.0 A Max, V~, Hz, CI. I Type of Manufacturer s Testing Laboratories used Type de programme du laboratoire d essais constructeur Model / Type Ref. Ref. De type MBC120-1XXXL-YYY-W Additional information (if necessary may also be reported on page 2) Les informations complémentaires (si nécessaire, peuvent être indiqués sur la deuxième page A sample of the product was tested and found to be in conformity with Un échantillon de ce produit a été essayé et a été considéré conforme à la As shown in the Test Report Ref. No. which forms part of this Certificate Comme indiqué dans le Rapport dessais numéro de référence qui constitue partie de ce Certificat Output rating see test report. In model name, the "X" and "Y" = 0-9, A-Z, a- z or blank, W is blank for Cl. I Additional information on page 2 IEC (ed.3);am This CB Test Certificate is issued by the National Certification Body Ce Certificat dessai OC est établi par l'organisme National de Certification Gaustadalléen 30 NO-0373 Oslo, Norway Date: Signature: Juan Z. Kleppenes Certification Department Issued /1

6 Ref. Certif. No. NO89050 IEC SYSTEM FOR MUTUAL RECOGNITION OF TEST CERTIFICATES FOR ELECTRICAL EQUIPMENT (IECEE) CB SCHEME SYSTEME CEI DACCEPTATION MUTUELLE DE CERTIFICATS DESSAIS DES EQUIPEMENTS ELECTRIQUES (IECEE) METHODE OC CB TEST CERTIFICATE CERTIFICAT D'ESSAI OC Product Produit Name and address of the applicant Nom et adresse du demandeur Name and address of the manufacturer Nom et adresse du fabricant Name and address of the factory Nom et adresse de l'usine Note: When more than one factory, please report on page 2 Note: Lorsque il y plus d'une usine, veuillez utiliser la deuxième page Ratings and principal characteristics Valeurs nominales et caractéristiques principales Trademark (if any) Marque de fabrique (si elle existe) Medical power supply for ( building-in ) EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez Andheri (East), Mumbai India EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez Andheri (East), Mumbai India EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez Andheri (East), Mumbai India Additional information on page 2 AC Input: 2.0A Max V~ 47-63Hz, CI. I Type of Manufacturer s Testing Laboratories used Type de programme du laboratoire d essais constructeur Model / Type Ref. Ref. De type MBC75-1XXXL-YYY-W Additional information (if necessary may also be reported on page 2) Les informations complémentaires (si nécessaire, peuvent être indiqués sur la deuxième page A sample of the product was tested and found to be in conformity with Un échantillon de ce produit a été essayé et a été considéré conforme à la As shown in the Test Report Ref. No. which forms part of this Certificate Comme indiqué dans le Rapport dessais numéro de référence qui constitue partie de ce Certificat Output rating see test report. In model name, the "X" and "Y" = 0-9, A-Z, a- z or blank, W is blank for Cl. I Additional information on page 2 IEC (ed.3);am This CB Test Certificate is issued by the National Certification Body Ce Certificat dessai OC est établi par l'organisme National de Certification Gaustadalléen 30 NO-0373 Oslo, Norway Date: Signature: Juan Z. Kleppenes Certification Department Issued /1

7 Test Report issued under the responsibility of IEC Medical electrical equipment Part 1: General requirements for basic safety and essential performance Report Reference No.... : Date of issue... : 23 October 2015 Total number of pages... : 223 CB Testing Laboratory... : Nemko USA Inc. Phone: Address... : Applicant s name... : Address... : 2210 Faraday Avenue, Suite 150, Carlsbad, CA 92008, USA EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez, Andheri (E), Mumbai, , India Test specification: Standard...: Test procedure...: Non-standard test method..: Test Report Form No....: Test Report Form Originator...: IEC : CORR. 1: CORR. 2: AM1:2012 (or IEC : 2012 reprint) CB Scheme N/A IEC60601_1J UL(US) Master TRF... : Copyright 2014 Worldwide System for Conformity Testing and Certification of Electrotechnical Equipment and Components (IECEE), Geneva, Switzerland. All rights reserved. This publication may be reproduced in whole or in part for non-commercial purposes as long as the IECEE is acknowledged as copyright owner and source of the material. IECEE takes no responsibility for and will not assume liability for damages resulting from the reader's interpretation of the reproduced material due to its placement and context. If this Test Report Form is used by non-iecee members, the IECEE/IEC logo and the reference to the CB Scheme procedure shall be removed. This report is not valid as a CB Test Report unless signed by an approved CB Testing Laboratory and appended to a CB Test Certificate issued by an NCB in accordance with IECEE 02. General disclaimer: The test results presented in this report relate only to the object tested. This report shall not be reproduced, except in full, without the written approval of the Issuing CB testing laboratory. The authenticity of this Test Report and its contents can be verified by contacting the NCB, responsible for this Test Report. This Test Report, when bearing the Nemko name and logo is only valid when issued by a Nemko laboratory, or by a laboratory having special agreement with Nemko.

8 Page 2 of 222 Report No Test item description... : Trade Mark... : Medical Power Supply (for building-in) Manufacturer...: EOS Power India PVT Ltd. Model/Type reference...: LFMWLP120-1XXX-YYY-W, LFMWLP75-1XXX-YYY-W LFMWLP65-1XXX-YYY-W or LFMWLP45-1XXX-YYY-W, (Where: "X" (first) = 0 or 3; "XX" (second and third) = 01 to 99; "Y" = 0-9, A-Z, a-z or blank, W is blank for MOPP or 1 for MOOP for Class I ) For Bel Power Solutions & Protection, a bel group: MBC120-1XXXL-YYY-W or MBC75-1XXXL-YYY-W (Where: "X" and "Y" = 0-9, A-Z, a-z or blank, W is blank for Class I ) Ratings...: AC Input: 3.0 A Max, V~, Hz (For Models LFMWLP120-1XXX-YYY W and MBC120-1XXXL- YYY-W ) or AC Input: 2.0 A Max, V~, Hz (For Models LFMWLP75-1XXX-YYY-W, LFMWLP65-1XXX-YYY- W, LFMWLP45-1XXX-YYY-W, MBC75-1XXXL-YYY-W) Output: Refer to General Product Information, Class I. and Testing procedure and testing location: CB Testing Laboratory: Testing location/ address... : Nemko USA Inc Faraday Ave. Suite 150, Carlsbad, CA 92008, USA Associated CB Testing Laboratory: Testing location/ address... : Tested by (name + signature)... : Jeff Busch Approved by (name + signature)... : David Atkinson

9 Page 3 of 222 Report No List of Attachments (including a total number of pages in each attachment): Document Appended 1: Photographs (Page number #179) Document Appended 2: PCB trace layouts (Page number #181) Document Appended 3: Circuit diagrams (Page number #184) Document Appended 4: Transformer and Inductor drawings (Page number #185) Attachment 1: National differences (22 pages) Attachment 2: Installation instructions (2 page) Summary of testing: Clause Requirement + Test All Information about the standards, documents considered Comment European Countries EN (2006) +A11 (2011) + AM1:2013 +AC:2014 +A12:2014. Refer also to National Differences attachment.1 All General The equipment is an open-frame, Class I switch mode power supply with universal AC input and multiple DC voltage outputs for building-in. This report covers multiple models and all comments / tests apply to all models unless otherwise indicated. Testing was conducted on various models as indicated. All General Unless otherwise noted, testing in this report covers worstcase testing on 12V (LFMWLP ), 12V (LFMWLP ) and 58V ( LFMWLP ) (LFMWLP ) output units, which is considered representative of the other models. All Risk Management The manufacturer performed the Risk Management process according to ISO 14971, 2 nd edition. All Rated ambient temperature range The power supply has been evaluated for 50 C when fully rated and de-rated at 70 C ambient as well as 85V (-15% tolerance) and 100V rating, temperatures as noted within this report. The Tmra must be checked when the equipment is built in an end product, or forms a part of a complete system. 4.3 Essential performance functions identified according to manufacturer s policy for risk acceptability in risk management file Essential performance shall be determined when installed in the end-use equipment as part of the risk management process for the end product. 4.5 Equvalent safety The optocouplers (U2) have been separately tested and approved to the relevant component standard, (EN ) by VDE. The component certification is considered to provide equivalent safety for two means of patient protection (2 MOPPs), refer to Insulation Diagram for defined patient protection. The PCB, transformer and bridging Ycapacitors comply with IEC (ed.3) requirements for patient protection

10 Page 4 of 222 Report No Summary of testing: Clause Requirement + Test 4.6 Risk management process identifies parts that can come into contact with patient but not defined as applied parts subjected to the requirements for applied parts, except for ME equipment remained single fault safe, or the risk remained acceptable as determined by 4.2 Comment Output of the PSU was not evaluated nor was it considered for direct contact to the patient; additional evaluation will be required in the end installation. The power supply output (secondary to ground) was evaluated as providing 1 250V and also providing 2 MOPP at 58Vdc, additionally the required Clearance value was increased to 4.0mm by request of the manufacturer for BF output consideration. The insulation was evaluated according to both Means of Operator Protection (MOOP), and Means of Patient Protection (MOPP), refer to General product information. Risk considered as part of this evaluation, refer to RM Results appended table Components of ME equipment The equipment is evaluated as MOPP and MOOP the only difference is the bridging components used the PCB layous and distances on the PCB are the same. For MOPP - The optocouplers (U2) have been separately tested and approved to the relevant component standard (EN ) by VDE. The component certification is considered to provide equivalent safety for two means of patient protection (2 MOPPs), refer to Insulation Diagram for defined operator and patient protection. The primary to secondary capacitors are 2 Y1 capcitors in series. For MOOP - The optocouplers (U2) that are not approved to are only considered as providing two means of operator protection (2 MOOP s). The primary to secondary capacitor can be a single Y1 capacitor. Acceptance of the optocoupler is at the discretion of the accepting NCB or agency. The PCB and transformer comply with IEC (ed.3) requirements for patient protection. 5.9 Determination of applied parts and accessible parts 7 Identification, markings and documents Output of the PSU was not evaluated nor was it considered for direct contact to the patient, additional evaluation will be required in the end installation. The power supply output (secondary to ground) was evaluated as providing 1 250V and also providing 2 MOPP at 58Vdc, additionally the required Clearance value was increased to 4.0mm by request of the manufacturer for BF output consideration. The insulation was evaluated according to both Means of Operator Protection (MOOP), and Means of Patient Protection (MOPP). Instructions and marking related to safety shall be in a language which is acceptable in the country in which the equipment is to be sold. English version evaluated. 7.9 Accompanying documents The equipment is a PSU for building-in. The end product evaluation shall ensure that the requirements related to accompanying documents complying with this standard are met in which is provided in the language required for the market where the equipment is sold.

11 Page 5 of 222 Report No Summary of testing: Clause Requirement + Test Comment 8.3 Classification of applied parts Output of the PSU was not evaluated nor was it considered for direct contact to the patient; additional evaluation will be required in the end installation. The power supply output (secondary to ground) was evaluated as providing 1 250V and also providing 2 MOPP at 58Vdc, additionally the required Clearance value was increased to 4.0mm by request of the manufacturer for BF output consideration. The insulation was evaluated according to both Means of Operator Protection (MOOP), and Means of Patient Protection (MOPP). 8.4 Limitation of voltage, current or energy Accessible part including applied parts. 8.5 Separation of Parts - Means of Protection (MOP) F-type Applied Part isolation (MOPP) Output does not exceeded 240VA, therefore the output is considered not to be an energy hazard. The equipment is a PSU for building-in. To be further evaluated in the end use product. The output has not been evaluated for direct patient connection. Suitability is to be evaluated in the end application. The insulation was evaluated according to Means of Patient Protection (MOPP) and additionally as means of operator protection (MOOP). Output of the PSU was not evaluated nor was it considered for direct contact to the patient; additional evaluation will be required in the end installation. The power supply output (secondary to ground) was evaluated as providing 1 250V and also providing 2 MOPP at 58Vdc, additionally the required Clearance value was increased to 4.0mm by request of the manufacturer for BF output consideration. Therefore, the secondary working voltages were evaluated to be the maximum mains voltage to achieve patient protection (MOPP) Defibrillation proof applied parts The manufacturer does not specify that the equipment is provided with a defibrillation proof applied part. 8.7 Leakage currents and patient auxiliary currents 8.9 Creepage distances and air clearances Creepage distances and air clearances complying with IEC The equipment is a PSU for building-in. Earth and touch leakage current, (patient and voltage on applied part conducted by the request of manufacturer) were performed. To be re-evaluated when installed in the end product. The equipment is a PSU for building-in. The creepage and clearance distance need to be evaluated when installed in the end equipment. MOPP or MOOP Optocouplers have been separately identified in appended table Optocouplers accepted for MOOP based on IEC certification Mains fuses Low-breaking capacity fusing is considered adequate based on a diode bridge (D1) short circuit current that measured less than 10 times the fusing rating with the use of (RT1) and (L1) components. Additionally the primary common-mode inductor (L1) component separately passed a 1 MOPP dielectric strength test, refer to appended table Construction acceptance is at the discretion of the receiving agency.

12 Page 6 of 222 Report No Summary of testing: Clause Requirement + Test 11.1 Protection against excessive temperatures and other hazards Maximum temperature during normal use 11.3b Constructional requirements for fire enclosures of ME equipment 11.7 ME equipment, ME system, and accessories coming into direct or indirect contact with biological tissues, cells, or body fluids assessed and documented according to ISO Electromagnetic compatibility of ME equipment and ME systems Comment This report covers a series of power supply models. Testing was performed on various models as indicated in this report. This testing was considered representative for all models. Unless otherwise stated, all tests were performed on worstcase model. The Tma for the maximum output rating is 50 C for most models. Power supplies can operate in up to a 70 C ambient with a derated output load, refer to General product information and appended table The equipment is a PSU for building-in which provide >15W output. The PSU must be provided with a suitable fire enclosure. The fire enclosure shall be evaluated in the end product. The equipment is a PSU for building-in. The end-use equipment must be evaluated to determine compliance with the requirements of ISO The equipment is a component level power supply for building-in, the requirements to this clause have to be evaluated in the end product. Additionally, the equipment has been evaluated for the requirements of IEC as a component power supply. Documentation is maintained by the manufacturer. Tests performed (name of test and test clause): Testing location: See Page : Power input 5.7: Humidity and preconditioning treatment 7.1.3: Durability of marking 8.4.2: Working voltage / Power measurement 8.4.3: Plug-measurement of voltage Protective earthing 8.7: Leakage current 8.8.3: Dielectric strength : Mechanical strength and resistance to heat 11.1: Excessive temperatures 11.8: Interruption of power supply 13.2: Single fault conditions 15.5: Transformers Summary of compliance with National Differences List of countries addressed: All CENELEC members according EN (2006) +A11 (2011) + AM1:2013 +AC:2014 +A12:2014.The list of countries recognizing the CB Scheme is actively updated on the IECEE website. ( All CB members as listed in the IECEE Online Bulletin Canada, Switzerland, Japan, Korea, United States. The product fulfils the requirements of IEC/EN Edition AM1

13 Page 7 of 222 Report No Copy of marking plate The artwork below may be only a draft. The use of certification marks on a product must be authorized by the respective NCBs that own these marks. EOS LFMWLP120-1XXXX-YYY-W (representative of other models not shown)

14 Page 8 of 222 Report No Copy of marking plate The artwork below may be only a draft. The use of certification marks on a product must be authorized by the respective NCBs that own these marks. EOS LFMWLP120-1XXXX-YYY-W (representative of other models not shown)

15 Page 9 of 222 Report No Copy of marking plate The artwork below may be only a draft. The use of certification marks on a product must be authorized by the respective NCBs that own these marks. EOS LFMWLP75-1XXXX-YYY-W (representative of other models not shown)

16 Page 10 of 222 Report No Copy of marking plate The artwork below may be only a draft. The use of certification marks on a product must be authorized by the respective NCBs that own these marks. EOS LFMWLP75-1XXXX-YYY-W (representative of other models not shown)

17 Page 11 of 222 Report No Copy of marking plate The artwork below may be only a draft. The use of certification marks on a product must be authorized by the respective NCBs that own these marks. EOS LFMWLP65-1XXXL (representative of other models not shown) EOS LFMWLP45-1XXXX-YYY-W (representative of other models not shown)

18 Page 12 of 222 Report No Copy of marking plate The artwork below may be only a draft. The use of certification marks on a product must be authorized by the respective NCBs that own these marks. Bel MBC120-1XXXL (representative of other models not shown)

19 Page 13 of 222 Report No Calibration Measurement uncertainty Evaluation of results All instruments used in the tests given in this test report are calibrated and traceable to national or international standards. Further information about traceability will be given on request. Measurement uncertainties are calculated for all instruments and instrument set-ups given in this report. Calculations are based on the principles given in the standard EA-4/02 (Dec. 1999), IEC Guide 115:2007 and other relevant internal Nemko-procedures. Further information about measurement uncertainties will be given on request. If not explicitly stated otherwise in the standard, the test is passed if the measured value is equal to or below (above) the limit line, regardless of the measurement uncertainty. If the measured value is above (below) the limit line, the test is not passed - ref IEC Guide 115:2007. The instrumentation accuracy is within limits agreed by IECEE-CTL.

20 Page 14 of 222 Report No GENERAL INFORMATION Test item particulars (see also Clause 6): Classification of installation and use... : Device type (component/sub-assembly/ equipment/ system)... : Intended use (Including type of patient, application location)... : Mode of operation... : Supply connection... : Accessories and detachable parts included... : Other options include... : Testing Class I, PSU for building-in Component, PSU for building-in PSU for building-in Continuous PSU for building-in None None Date of receipt of test item(s)... : September, 2015 Dates tests performed... : July August, 2015 Possible test case verdicts: - test case does not apply to the test object... : N/A - test object does meet the requirement... : Pass (P) - test object was not evaluated for the requirement... : N/E (collateral standards only) - test object does not meet the requirement... : Fail (F) Abbreviations used in the report: - normal condition...: N.C. - single fault condition...: S.F.C. - means of Operator protection...: MOOP - means of Patient protection...: MOPP General remarks: "(See Attachment #)" refers to additional information appended to the report. "(See appended table)" refers to a table appended to the report. The tests results presented in this report relate only to the object tested. This report shall not be reproduced except in full without the written approval of the testing laboratory. List of test equipment must be kept on file and available for review. Additional test data and/or information provided in the attachments to this report. Throughout this report a comma / point is used as the decimal separator. Manufacturer s Declaration per sub-clause of IECEE 02: The application for obtaining a CB Test Certificate includes more than one factory location and a declaration from the Manufacturer stating that the sample(s) submitted for evaluation is (are) representative of the products from each factory has been provided... : Yes Not applicable When differences exist; they shall be identified in the General product information section. Name and address of factory (ies)... : EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez, Andheri (East), Mumbai , India

21 Page 15 of 222 Report No General product information: LFMWLP120-ZXXX-YYY-W is a series of open frame Class I switch mode power supply intended for building in in medical equipment end-products. The model series has an input range of V ac, with manufacturer tolerances of -15% to +10% (ranging from V ac). The model series has single output voltage ranging from 12 to 58V dc. The model series is rated at 120W maximum. The equipment is provided with a PCB-mount molex- type input connector (or equivalent). All models of LFMWLP120-1XXX-YYY-W series are identical, except for the mains transformer (T1) and minor secondary components changes that allow for different output voltage ratings. This test report covers series of models as follows:eos Corporation: Models are LFMWLP120-1XXX-YYY-W, LFMWLP45-1XXX-YYY-W, LFMWLP65-1XXX-YYY-W, and LFMWLP75-1XXX-YYY-W; and Bel Power Solutions & Protection, a Bel group: Models MBC120-1XXXL-YYY-W,and ABC75-1XXXL-YYY-W. The following are optional configurations for all models: 1) Power supply can be provided as MOPP or MOOP, the only differences are the bridging components used, the PCB layouts are the same for both configurations. For MOPP 2 Y1 capacitors in series between primary to secondary, opto-couplers are certified according to IEC and a single Y capacitor is provided from mains to ground (Y1 or Y2) and optionally from secondary to ground (Y1 for 2 MOPP or Y2 for 1 MOPP). For MOOP - 2 Y1 capacitors in series or a single Y1 capacitor between primary to secondary, opto-couplers are certified according to IEC or IEC and a single Y capacitor is provided from mains to ground (Y1 or Y2) and optionally from secondary to ground. 2) The bridging capacitor (depending on MOP, primary to secondary) can be two capacitors or a single capacitor, when single capacitor is provided it is populated in to outer two components pads with midpoint not populated, and is the same values as the total of 2 capacitors. 3) MOV (MV1) is optional. 4) Inductor L5 is optional component provided in protective earth path (on mains section of board) Model differences: For EOS Models LFMWLP120-1XXX-YYY-W, LFMWLP45-1XXX-YYY-W, LFMWLP65-1XXX-YYY-W, and LFWLP75-1XXX-YYY-W. The X (first) = number 0 or 3 denoting type of connector (0- for screw terminal; 3- Header type); XX (second and third) = numbers 01 to 99 denoting output voltage; Y = could be 0-9, AZ, a-z or blank; YYY denotes minor difference and do not effect safety characteristics. Alternative trademark Bel Power Solution is added to this EOS LFMWLP120/75 series with the same construction. The only difference is in the makings for marketing purposes. Testing on the EOS models is representative of the Bel Power Solution models. See table below for examples of equivalent EOS to Bel Power Solution model designations. For Bel Power, Models MBC120-1XXXL-YYY-W or MBC75-1XXXL-YYY-W. The character "X" and "Y" = 0-9, A-Z, a-z or blank. Model correlation to EOS Models are listed in the below table. The model designation variables for Bel Power Solution are defined as follows: X = any alpha or numeric from 0-9 (representing the output voltage) Y = any alpha or numeric character or blank (denotes minor output variation and /or minor SELV circuit variations). W may be blank or 1 with blank denoting models provided with Y1-type capacitors (C33 and C38) bridging mains to secondary (2 MOPP), or 1 denoting models provided with single Y1-type capacitor (C33 or C38 )bridging mains to secondary (2 MOOP); Model LFMWLP120 provides up to 100W when convection cooled and up to 120W when force cooled with 300 LFM air flow. Model LFMWLP75 provides 75W, Model LFMWLP65 provides 65W, and Model LFMWLP45 provides 45W, all models when convection cooled. All models are similar except for output rating, model designation; Transformer (T1) secondary winding and other secondary components. The parameters of these components can be adjusted to obtain corresponding output power and output current. Tma is 50 C or 70 C (with de-rated output). This Report covers an entire series. Refer to appended table for models tested.

22 Page 16 of 222 Report No General product information: These are component power supply intended for building-in Class I or Class II end-products. The MWLP series has single output versions whose voltage can be from 12VDC to 58VDC.The power supplies deliver full power up to +50 C and will operate at up to +70 C with derating. LFMWLP120 provides up to 100W when convection cooled and up to 120 W when force cooled with 300 LFM air flow applied to inductor L3 inward. The LFMWLP75 provides 75W when convection cooled. Condition Voltage Current Load Input range Colling Tma ( C) Output Status used Model LFMWLP (Rated 3.0A max., Vac, Hz) A V~ 300LFM 50 Forced B V~ 300LFM 70 Forced C V~ Natural 50 D V~ Natural 70 E <100V~ Natural 50 F <100V~ Natural 70 LFMWLP ((Rated 3.0A max., Vac, Hz) G V~ 300LFM 50 Forced H V~ 300LFM 70 Forced I V~ Natural 50 J V~ Natural 70 K <100V~ Natural 50 L <100V~ Natural 70 LFMWLP (Rated 2.0A max., Vac, Hz) A V~ Natural 50 B V~ Natural 70 C <100V~ Natural 50 D <100V~ Natural 70 LFMWLP (Rated 2.0A max., Vac, Hz) E V~ Natural 50 F V~ Natural 70 G <100V~ Natural 50 H <100V~ Natural 70

23 Page 17 of 222 Report No General product information: Letter references in the above table (A to H1) indicates loading condition as noted in the table below. Mentioned below is representative Model Ratings Table for 50 C ambient with 300 LFM air flow from Boost inductor L3.Derated power ratings at 70 C ambient are also specified below: The alphabets in parenthesis represent the overall series loading. Model: LFMWLP120-ZXXX-YYY-W Output Ratings for Input range: 85Vac-264Vac Maximum Individual Continuous Power with 300LFM Forced Air flow & MODEL Power Derating at Elevated Temperatures Voltage 50 C 70 C Volts Watts Watts LFMWLP (A) 60(B) LFMWLP LFMWLP LFMWLP LFMWLP LFMWLP (G) 60(H) Output Ratings for Convection Cooling Input range: 100Vac-264Vac Maximum Individual Continuous Power with Input range: 85Vac - <100Vac Maximum Individual Continuous Power with MODEL Convection cooling & Power Derating at Convection cooling & Power Derating at Elevated Temperatures Elevated Temperatures Voltage 50 C 70 C 50 C 70 C Volts Watts Watts Watts Watts LFMWLP (C) 50(D) 80(E) 40(F) LFMWLP LFMWLP LFMWLP LFMWLP LFMWLP (I) 50(J) 80(K) 40 (L) Model: LFMWLP75-ZXXX-YYY-W Output Ratings for Input range: Vac Maximum Individual Continuous Power with Convection cooling & Power MODEL Derating at Elevated Temperatures Voltage 50 C 70 C Volts Watts Watts LFMWLP (A1) 37.5(B1) LFMWLP LFMWLP LFMWLP LFMWLP LFMWLP (E1) 37.5 (F1)

24 Page 18 of 222 Report No General product information: Output Ratings for Input range: 85 - <100Vac Maximum Individual Continuous Power with Convection cooling & Power MODEL Derating at Elevated Temperatures Voltage 50 C 70 C Volts Watts Watts LFMWLP (C1) 32.5(D1) LFMWLP LFMWLP LFMWLP LFMWLP LFMWLP (G1) 32.5 (H1) The clearance distances have additionally been assessed for suitability up to 5000m elevation. All models have identical schematic and PWB layout

25 Page 19 of 222 Report No IEC Clause Requirement + Test Result - Remark Verdict General product information: Custo EOS Bel m Voltage Current Part Model Number Connector Part Number Suffix LFMWLP V 10A MBC120-1T12L LFMWLP Header MBC L LFMWLP V 8A MBC120-1T15L LFMWLP Header MBC L LFMWLP V 5A MBC120-1T24L LFMWLP Header MBC L LFMWLP V 2.5A MBC120-1T48L LFMWLP Header MBC L LFMWLP V 4A MBC120-1T30L LFMWLP Header MBC L LFMWLP V 2.06A MBC120-1T58L LFMWLP Header MBC L LFMWLP V 6.25A MBC75-1T12L LFMWLP Header MBC L LFMWLP V 5.00A MBC75-1T15L LFMWLP Header MBC L LFMWLP V 3.13A MBC75-1T24L LFMWLP Header MBC L LFMWLP V 1.56A MBC75-1T48L LFMWLP Header MBC L LFMWLP V 2.50A MBC75-1T30L

26 Page 20 of 222 Report No IEC Clause Requirement + Test Result - Remark Verdict General product information: LFMWLP Header MBC L LFMWLP V 1.29A MBC75-1T58L LFMWLP Header MBC L LFMWLP LFMWLP Header 12V 5.42A LFMWLP LFMWLP Header 15V 4.33A LFMWLP LFMWLP Header 24V 2.71A LFMWLP LFMWLP Header 48V 1.35A LFMWLP LFMWLP Header 30V 2.17A LFMWLP LFMWLP Header 58V 1.12A LFMWLP LFMWLP Header 12V 3.75A LFMWLP LFMWLP Header 15V 3.00A LFMWLP LFMWLP Header 24V 1.88A LFMWLP LFMWLP Header 48V 0.94A

27 Page 21 of 222 Report No IEC Clause Requirement + Test Result - Remark Verdict General product information: LFMWLP LFMWLP Header 30V 1.50A LFMWLP LFMWLP Header 58V 0.78A

28 λºò Ý» ºò Ò±ò ÒÑèçðêí ÛÝ ÍÇÍÌÛÓ ÚÑÎ ÓËÌËßÔ ÎÛÝÑÙÒ Ì ÑÒ ÑÚ ÌÛÍÌ ÝÛÎÌ Ú ÝßÌÛÍ ÚÑÎ ÛÔÛÝÌÎ ÝßÔ ÛÏË ÐÓÛÒÌ ø ÛÝÛÛ ÝÞ ÍÝØÛÓÛ ÍÇÍÌÛÓÛ ÝÛ ÜßÝÝÛÐÌßÌ ÑÒ ÓËÌËÛÔÔÛ ÜÛ ÝÛÎÌ Ú ÝßÌÍ ÜÛÍÍß Í ÜÛÍ ÛÏË ÐÛÓÛÒÌÍ ÛÔÛÝÌÎ ÏËÛÍ ø ÛÝÛÛ ÓÛÌØÑÜÛ ÑÝ ÝÞ ÌÛÍÌ ÝÛÎÌ Ú ÝßÌÛ ÝÛÎÌ Ú ÝßÌ ÜùÛÍÍß ÑÝ Ð ±¼«½ Ð ±¼«Ò ³» ²¼ ¼¼» ±º» ½ ² Ò±³» ¼»» ¼«¼»³ ²¼»«Ó»¼ ½ ±» «º± ø ¾«¼ ²¹ó ² Ò ³» ²¼ ¼¼» ±º» ³ ²«º ½ Ò±³» ¼»» ¼«º ¾ ½ ² Ò ³» ²¼ ¼¼» ±º» º ½ ± Ò±³» ¼»» ¼» ù«²» Ò±»æ É»² ³±» ² ±²» º ½ ± ô»»» ± ±² ¹» î Ò±»æ Ô± «¼ù«²» «²»ô ª» ¼»«8³» ¹» Î ²¹ ²¼ ²½ ½ ½» ½ Ê»«²±³ ²»» ½ ½ 7 ²½» Ì ¼»³ µ ø º ² Ó ¼» º ¾ ø»»»» ß¼¼ ±² ²º± ³ ±² ±² ¹» î îòð ß Ó ô ïððóîìð Ê ìéóêí Ø ô Ý ò Ì» ±º Ó ²«º ½ Ì» ²¹ Ô ¾± ±» ¼ Ì» ¼» ±¹ ³³» ¼«¾± ±» ¼» ½±² «½»«Ó±¼» ñ Ì» λºò λºò Ü»» ß¼¼ ±² ²º± ³ ±² ø º ²»½» ³ ± ¾»» ±»¼ ±² ¹» î Ô» ²º± ³ ±² ½±³ 7³»²» ø ²7½»»ô»«ª»² 6» ²¼ «7 «¼»«8³» ¹» ß ³» ±º» ±¼«½»»¼ ²¼ º±«²¼ ± ¾» ² ½±²º± ³ ˲ 7½ ² ±² ¼» ½» ±¼«7 7» 7» 7 7 ½±² ¼7 7 ½±²º± ß ± ² ²» Ì» λ ± λºò Ò±ò ½ º± ³ ±º Ý» º ½» ݱ³³» ²¼ «7 ¼ ²» Î ± ¼» ²«³7 ± ¼» 7º7»²½» «½±² » ¼» ½» Ý» º ½ ÓÞÝéëóïÈÈÈÔóÇÇÇóî Ñ««²¹»»»»» ± ò ² ³±¼» ² ³»ô» þèþ ²¼ þçþ ã ðóçô ßó Æô ó ± ¾ ²µ ß¼¼ ±² ²º± ³ ±² ±² ¹» î ÛÝ êðêðïóïø»¼òí å ³ï îçìîçé Ì ÝÞ Ì» Ý» º ½» ¼ ¾» Ò ±² Ý» º ½ ±² Þ±¼ Ý» Ý» º ½ ¼» ÑÝ» 7 ¾ ùñ ¹ ² ³» Ò ±² ¼» Ý» º ½ ±² Ù «¼ 7»² íð ÒÑóðíéí Ñ ±ô Ò± Ü»æ îèóïðóîðïë Í ¹² æ Ö«² Æò Õ»»²» Ý» º ½ ±² Ü» ³»² ¼ îððéóðì ïñï

29 λºò Ý» ºò Ò±ò ÒÑèçðêì ÛÝ ÍÇÍÌÛÓ ÚÑÎ ÓËÌËßÔ ÎÛÝÑÙÒ Ì ÑÒ ÑÚ ÌÛÍÌ ÝÛÎÌ Ú ÝßÌÛÍ ÚÑÎ ÛÔÛÝÌÎ ÝßÔ ÛÏË ÐÓÛÒÌ ø ÛÝÛÛ ÝÞ ÍÝØÛÓÛ ÍÇÍÌÛÓÛ ÝÛ ÜßÝÝÛÐÌßÌ ÑÒ ÓËÌËÛÔÔÛ ÜÛ ÝÛÎÌ Ú ÝßÌÍ ÜÛÍÍß Í ÜÛÍ ÛÏË ÐÛÓÛÒÌÍ ÛÔÛÝÌÎ ÏËÛÍ ø ÛÝÛÛ ÓÛÌØÑÜÛ ÑÝ ÝÞ ÌÛÍÌ ÝÛÎÌ Ú ÝßÌÛ ÝÛÎÌ Ú ÝßÌ ÜùÛÍÍß ÑÝ Ð ±¼«½ Ð ±¼«Ò ³» ²¼ ¼¼» ±º» ½ ² Ò±³» ¼»» ¼«¼»³ ²¼»«Ó»¼ ½ ±» «º± ø ¾«¼ ²¹ó ² Ò ³» ²¼ ¼¼» ±º» ³ ²«º ½ Ò±³» ¼»» ¼«º ¾ ½ ² Ò ³» ²¼ ¼¼» ±º» º ½ ± Ò±³» ¼»» ¼» ù«²» Ò±»æ É»² ³±» ² ±²» º ½ ± ô»»» ± ±² ¹» î Ò±»æ Ô± «¼ù«²» «²»ô ª» ¼»«8³» ¹» Î ²¹ ²¼ ²½ ½ ½» ½ Ê»«²±³ ²»» ½ ½ 7 ²½» Ì ¼»³ µ ø º ² Ó ¼» º ¾ ø»»»» ß¼¼ ±² ²º± ³ ±² ±² ¹» î ßÝ ² «æ íòð ß Ó ïððó îìð Ê ìéó êí Ø ô Ý ò Ì» ±º Ó ²«º ½ Ì» ²¹ Ô ¾± ±» ¼ Ì» ¼» ±¹ ³³» ¼«¾± ±» ¼» ½±² «½»«Ó±¼» ñ Ì» λºò λºò Ü»» ß¼¼ ±² ²º± ³ ±² ø º ²»½» ³ ± ¾»» ±»¼ ±² ¹» î Ô» ²º± ³ ±² ½±³ 7³»²» ø ²7½»»ô»«ª»² 6» ²¼ «7 «¼»«8³» ¹» ß ³» ±º» ±¼«½»»¼ ²¼ º±«²¼ ± ¾» ² ½±²º± ³ ˲ 7½ ² ±² ¼» ½» ±¼«7 7» 7» 7 7 ½±² ¼7 7 ½±²º± ß ± ² ²» Ì» λ ± λºò Ò±ò ½ º± ³ ±º Ý» º ½» ݱ³³» ²¼ «7 ¼ ²» Î ± ¼» ²«³7 ± ¼» 7º7»²½» «½±² » ¼» ½» Ý» º ½ ÓÞÝïîðóïÈÈÈÔóÇÇÇóî Ñ««²¹»»»»» ± ò ² ³±¼» ² ³»ô» þèþ ²¼ þçþ ã ðóçô ßó Æô ó ± ¾ ²µ ß¼¼ ±² ²º± ³ ±² ±² ¹» î ÛÝ êðêðïóïø»¼òí å ³ï îçìîçé Ì ÝÞ Ì» Ý» º ½» ¼ ¾» Ò ±² Ý» º ½ ±² Þ±¼ Ý» Ý» º ½ ¼» ÑÝ» 7 ¾ ùñ ¹ ² ³» Ò ±² ¼» Ý» º ½ ±² Ù «¼ 7»² íð ÒÑóðíéí Ñ ±ô Ò± Ü»æ îèóïðóîðïë Í ¹² æ Ö«² Æò Õ»»²» Ý» º ½ ±² Ü» ³»² ¼ îððéóðì ïñï

30 Test Report issued under the responsibility of IEC Medical electrical equipment Part 1: General requirements for basic safety and essential performance Report Reference No.... : Date of issue... : 27 October 2015 Total number of pages... : 222 CB Testing Laboratory... : Nemko USA Inc. Phone: Address... : Applicant s name... : Address... : 2210 Faraday Avenue, Suite 150, Carlsbad, CA 92008, USA EOS Power India PVT Ltd. Unit #57, SDF II, Seepz-Sez, Andheri (E), Mumbai, , India Test specification: Standard...: Test procedure... : Non-standard test method..: Test Report Form No....: Test Report Form Originator...: IEC : CORR. 1: CORR. 2: AM1:2012 (or IEC : 2012 reprint) CB Scheme N/A IEC60601_1J UL(US) Master TRF... : Copyright 2014 Worldwide System for Conformity Testing and Certification of Electrotechnical Equipment and Components (IECEE), Geneva, Switzerland. All rights reserved. This publication may be reproduced in whole or in part for non-commercial purposes as long as the IECEE is acknowledged as copyright owner and source of the material. IECEE takes no responsibility for and will not assume liability for damages resulting from the reader's interpretation of the reproduced material due to its placement and context. If this Test Report Form is used by non-iecee members, the IECEE/IEC logo and the reference to the CB Scheme procedure shall be removed. This report is not valid as a CB Test Report unless signed by an approved CB Testing Laboratory and appended to a CB Test Certificate issued by an NCB in accordance with IECEE 02. General disclaimer: The test results presented in this report relate only to the object tested. This report shall not be reproduced, except in full, without the written approval of the Issuing CB testing laboratory. The authenticity of this Test Report and its contents can be verified by contacting the NCB, responsible for this Test Report. This Test Report, when bearing the Nemko name and logo is only valid when issued by a Nemko laboratory, or by a laboratory having special agreement with Nemko.

31 Page 2 of 221 Report No Test item description... : Trade Mark... : Medical Power Supply (for building-in) Manufacturer...: EOS Power India PVT Ltd. Model/Type reference...: LFMWLP120-1XXX-YYY-II, LFMWLP75-1XXX-YYY-II LFMWLP65-1XXX-YYY-II or LFMWLP45-1XXX-YYY-II, (Where: "X" (first) = 0 or 3; "XX" (second and third) = 01 to 99; "Y" = 0-9, A-Z, a-z or blank) For Bel Power Solutions & Protection, a bel group: MBC120-1XXXL-YYY-2 or MBC75-1XXXL-YYY-2 (Where: "X" and "Y" = 0-9, A-Z, a-z or blank, ) Ratings...: AC Input: 3.0 A Max, V~, Hz (For Models LFMWLP120-1XXX-YYY II and MBC120-1XXXL- YYY-2 ) or AC Input: 2.0 A Max, V~, Hz (For Models LFMWLP75-1XXX-YYY-II, LFMWLP65-1XXX-YYY-II, LFMWLP45-1XXX-YYY-II, and MBC75-1XXXL-YYY-2) Output: Refer to General Product Information, Class II. Testing procedure and testing location: CB Testing Laboratory: and Nemko USA Inc. Testing location/ address... : 2210 Faraday Ave. Suite 150, Carlsbad, CA 92008, USA Associated CB Testing Laboratory: Testing location/ address... : Tested by (name + signature)... : Jeff Busch Approved by (name + signature)... : David Atkinson

32 Page 3 of 221 Report No List of Attachments (including a total number of pages in each attachment): Document Appended 1: Photographs (Page number #179) Document Appended 2: PCB trace layouts (Page number #181) Document Appended 3: Circuit diagrams (Page number #184) Document Appended 4: Transformer and Inductor drawings (Page number #185) Attachment 1: National differences (22 pages) Attachment 2: Installation instructions (2 page) Summary of testing: Clause Requirement + Test All Information about the standards, documents considered Comment European Countries, EN (2006) +A11 (2011) + AM1:2013 +AC:2014 +A12:2014. Refer also to National Differences attachment.1 All General The equipment is an open-frame, Class II switch mode power supply with universal AC input and multiple DC voltage outputs for building-in. This report covers multiple models and all comments / tests apply to all models unless otherwise indicated. Testing was conducted on various models as indicated. All General The LFMWLP120/75/65/45 series of power supplied are provided in both a Class I configuration (covered under separate test report) and a Class II configuration (covered in this test report). The only difference is that Inductance L5(optional), capacitance C2, C3, C5,C32, and protective earthing/bonding terminal M1 and M2; are not populated and the removal of the protective earth symbol next to the mounting pad. All traces and silk screening (component designations) are provided on the PCB for the depopulated components. To maintain Class II safety isolation, if needed in the end insulation, those mounting holes that are near hazardous parts (mains) need to be isolated from earth, secondary circuits and /or conductive accessible parts, by the use of standoffs of non-conductive material or other means. The safety isolation needs to be verified in the end installation. All General Unless otherwise noted, testing in this report covers worstcase testing on 12V (LFMWLP II 12V (LFMWLP II) and 58V ( LFMWLP II) (LFMWLP II ) output units, which is considered representative of the other models. All Risk Management The manufacturer performed the Risk Management process according to ISO 14971, 2 nd edition. All Rated ambient temperature range The power supply has been evaluated for 50 C when fully rated and de-rated at 70 C ambient as well as 85V (-15% tolerance) and 100V rating, temperatures as noted within this report. The Tmra must be checked when the equipment is built in an end product, or forms a part of a complete system.

33 Page 4 of 221 Report No Summary of testing: Clause Requirement + Test 4.3 Essential performance functions identified according to manufacturer s policy for risk acceptability in risk management file Comment Essential performance shall be determined when installed in the end-use equipment as part of the risk management process for the end product. 4.5 Equvalent safety The optocouplers (U2) have been separately tested and approved to the relevant component standard, (EN ) by VDE. The component certification is considered to provide equivalent safety for two means of patient protection (2 MOPPs), refer to Insulation Diagram for defined patient protection. The PCB, transformer and bridging Ycapacitors comply with IEC (ed.3) requirements for patient protection 4.6 Risk management process identifies parts that can come into contact with patient but not defined as applied parts subjected to the requirements for applied parts, except for ME equipment remained single fault safe, or the risk remained acceptable as determined by 4.2 Output of the PSU was not evaluated nor was it considered for direct contact to the patient; additional evaluation will be required in the end installation Risk considered as part of this evaluation, refer to RM Results appended table Components of ME equipment The equipment is evaluated as MOPP and MOOP the only difference is the bridging components used the PCB layous and distances on the PCB are the same. For MOPP - The optocouplers (U2) have been separately tested and approved to the relevant component standard (EN ) by VDE. The component certification is considered to provide equivalent safety for two means of patient protection (2 MOPPs), refer to Insulation Diagram for defined operator and patient protection. The primary to secondary capacitors are 2 Y1 capcitors in series. For MOOP - The optocouplers (U2) that are not approved to are only considered as providing two means of operator protection (2 MOOP s). The primary to secondary capacitor can be a single Y1 capacitor. Acceptance of the optocoupler is at the discretion of the accepting NCB or agency. The PCB and transformer comply with IEC (ed.3) requirements for patient protection. 5.9 Determination of applied parts and accessible parts 7 Identification, markings and documents Output of the PSU was not evaluated nor was it considered for direct contact to the patient, additional evaluation will be required in the end installation. Instructions and marking related to safety shall be in a language which is acceptable in the country in which the equipment is to be sold. English version evaluated. 7.9 Accompanying documents The equipment is a PSU for building-in. The end product evaluation shall ensure that the requirements related to accompanying documents complying with this standard are met in which is provided in the language required for the market where the equipment is sold.

34 Page 5 of 221 Report No Summary of testing: Clause Requirement + Test Comment 8.3 Classification of applied parts Output of the PSU was not evaluated nor was it considered for direct contact to the patient, additional evaluation will be required in the end installation. The power supply output (secondary to mounting hole M2) was evaluated as providing 1 250V and also providing 2 MOPP at 58Vdc, additionally the required Clearance value was increased to 4.0mm by request of the manufacturer for BF output consideration. The insulation was evaluated according to both Means of Operator Protection (MOOP), and Means of Patient Protection (MOPP). (Assumes mouting hole, M2 is connected to chassis) 8.4 Limitation of voltage, current or energy Accessible part including applied parts. 8.5 Separation of Parts - Means of Protection (MOP) F-type Applied Part isolation (MOPP) Output does not exceeded 240VA, therefore the output is considered not to be an energy hazard. The equipment is a PSU for building-in. To be further evaluated in the end use product. Output of the PSU was not evaluated nor was it considered for direct contact to the patient, additional evaluation will be required in the end installation. The power supply output (secondary to mounting hole M2) was evaluated as providing 1 250V and also providing 2 MOPP at 58Vdc, additionally the required Clearance value was increased to 4.0mm by request of the manufacturer for BF output consideration. The insulation was evaluated according to both Means of Operator Protection (MOOP), and Means of Patient Protection (MOPP). (Assumes mouting hole, M2 is connected to chassis) The insulation was evaluated according to Means of Patient Protection (MOPP) and additionally as means of operator protection (MOOP). Output of the PSU was not evaluated nor was it considered for direct contact to the patient, additional evaluation will be required in the end installation. The power supply output (secondary to mounting hole M2) was evaluated as providing 1 250V and also providing 2 MOPP at 58Vdc, additionally the required Clearance value was increased to 4.0mm by request of the manufacturer for BF output consideration. The insulation was evaluated according to both Means of Operator Protection (MOOP), and Means of Patient Protection (MOPP). (Assumes mouting hole, M2 is connected to chassis) Defibrillation proof applied parts The manufacturer does not specify that the equipment is provided with a defibrillation proof applied part. 8.7 Leakage currents and patient auxiliary currents 8.9 Creepage distances and air clearances The equipment is a PSU for building-in. Earth and touch leakage current, (patient and voltage on applied part conducted by the request of manufacturer) were performed. To be re-evaluated when installed in the end product. Output of the PSU was not evaluated nor was it considered for direct contact to the patient, additional evaluation will be required in the end installation. The power supply output (secondary to mounting hole M2) was evaluated as providing 1 250V and also providing 2 MOPP at 58Vdc, additionally the required Clearance value was increased to 4.0mm by request of the manufacturer for BF output consideration. The insulation was evaluated according to both Means of Operator Protection (MOOP), and Means of Patient Protection (MOPP). (Assumes mouting hole, M2 is connected to chassis)