Registration number (WIID)Project No.TitleStatus
42312LVS EN 50103:1995Guidance on aplication of EN 29001 and EN 46001 and EN 29002 and EN 46002 for the active (including active implantable) medical device industryAtcelts
63302LVS EN IEC 60601-2-39:2019Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipmentAtcelts
50385LVS EN 50061:1988Safety of implantable cardiac pacemakersAtcelts
45535LVS EN 60601-2-44:2002Medical electrical equipment - Part 2-44: Particular requirements for the safety of X-ray equipment for computed tomographyAtcelts
43932LVS EN 60601-2-45:2002Medical electrical equipment - Part 2-45: Particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devicesAtcelts
54479LVS HD 395.2.15 S1:2002Medical electrical equipment - Part 2: Particular requirements for the safety of capacitor discharge X-ray generatorsAtcelts
54294LVS EN 60601-2-37:2002Medical electrical equipment - Part 2-37: Particular requirements for the safety of ultrasonic medical diagnostic and monitoringAtcelts
44908LVS EN 60601-2-30:2002Medical electrical equipment - Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipmentAtcelts
50312LVS HD 513 S1:2002Determination of the maximum symmetrical radiation field from a rotating anode X-ray tube for medical diagnosisAtcelts
56968LVS EN 60601-2-2:2003Medical electrical equipment - Part 2-2: Particular requirements for the safety of high frequency surgical equipmentAtcelts
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