CLC/TC 62
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 51031 | LVS EN 60601-2-32:1994 | Medical electrical equipment - Part 2: Particular requirements for the safety of associated equipment of X-ray equipment | Atcelts |
| 42312 | LVS EN 50103:1995 | Guidance on aplication of EN 29001 and EN 46001 and EN 29002 and EN 46002 for the active (including active implantable) medical device industry | Atcelts |
| 53590 | LVS HD 395.2.9 S1:1989 | Medical electrical equipment - Part 2: Particular requirements for the safety of dosimeters used in radiotherapy with electrically-connected radiation detectors | Atcelts |
| 51989 | LVS EN 60601-2-33:1995/A11:1997 | Medical electrical equipment - Part 2: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis | Atcelts |
| 50559 | LVS HD 395.2.11 S2:1990 | Medical electrical equipment - Part 2: Particular requirements for the safety of gamma beam therapy equipment | Atcelts |
| 50174 | LVS HD 395.2.14 S1:1989 | Medical electrical equipment - Part 2: Particular requirements for the safety of electroconvulsive therapy equipment | Atcelts |
| 48922 | LVS HD 510 S1:1988 | Entrance field sizes of electro-optical X-ray image intensifiers | Atcelts |
| 50585 | LVS HD 395.2.12 S1:1989 | Medical electrical equipment - Part 2: Particular requirements for the safety of lung ventilators for medical use | Atcelts |
| 51998 | LVS EN 60601-2-16:2015 | Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment | Atcelts |
| 42171 | LVS EN 60601-2-49:2002 | Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment | Atcelts |
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