N60601-1 test report pdf

This report shall not be reproduced, except in full, without the written approval of the issuing cb testing laboratory. The use of certification marks on a product must be authorized by the respective ncbs that own these marks. The authenticity of this test report and its contents can be verified by contacting the ncb, responsible for this test report. If this test report form is used by noniecee members, the ieceeiec logo shall be removed. Test report iec 606011 en 60601 1 medical electrical equipment part 1. Iec 60601112 iectr 6060143 iectr 6060142 technical reports iectr 606014x. Abiocor implantable controller fcc corresp and phantom liquid info details for fcc id r9g00343340 made by abiomed inc document includes test report 00343340 implantable controller exposure. Test report iec 606011 en 60601 1 medical electrical. Highvoltage test ac single fault conditions n pc mains at application part din vde 07011 din vde 07021 din vde 07511 2001 dnei n606011 the foollwnig is measured. This report is not valid as a cb test report unless signed by an approved cb testing laboratory. This test report form can be used to complement the iec 60601 1 test report.

Refer to test report gzme150500045101relevant safety report iec 606011. Throughout this report a comma point is used as the decimal separator. The evaluation package is a summary of the iec 606011. Most problems in dental radiography are not the result of xray equipment. Customer authorization to perform tests according to this test plan. Acteon group and is the result of many years of experience in the radiology.

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. This test report form is intended for the evaluation of medical electrical equipment and medical electrical systems used in the home healthcare environment i n accordance with iec 60601111. Additional test data andor information provided in the attachments to this report. Wam2500 wireless acquisition module test report mortara wam. Structure of 60601 series those dashes matter n 606011 general. The product fulfils the requirements of iec 606011. The test has been performed according to the rear side conditions, which are. Test report iec 606011 medical electrical equipment part.

The test results presented in this report relate only to the object tested. Bosch and the symbol are registered trademarks of robert bosch gmbh, germany. Trf iec 606011h medical electrical equipment part 1 invacare. To do so, follow the procedure described in the manual of. Acteon group and is the result of many years of experience in the. General requirements for safety report reference no. What you need to know about medical electrical standards. Na k power output of auxiliary mains socketoutlets na l class ii symbol na. Test report en 60601 1 medical electrical equipment part.