Registration number (WIID)Project No.TitleStatus
50700EN 60601-2-23:2000Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipmentAtcelts
44650LVS HD 395.2.8 S1:1988Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray generatorsAtcelts
50826HD 395.2.11 S1:1989Medical electrical equipment - Part 2: Particular requirements for the safety of gamma beam therapy equipmentAtcelts
51806EN 60601-2-33:2002/A2:2008/corrigendum Nov. 2008Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosisAtcelts
51686EN 60601-1:1990/A12:1993/corrigendum Jul. 1994Medical electrical equipment - Part 1: General requirements for safetyAtcelts
58002EN 60601-2-26:2015Medical electrical equipment - Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographsAtcelts
51202LVS EN 60601-1-2:2008Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests (IEC 60601-1-2:2007, modified)Atcelts
55898EN 60601-2-23:2015Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipmentAtcelts
51950EN 60601-1-8:2004/A1:2006/corrigendum Oct. 2006Medical electrical equipment - Part 1-8: General requirements for safety - Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systemsAtcelts
56026HD 356 S1:1977Radiographic cassettesAtcelts
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