CLC/TC 62
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 50174 | HD 395.2.14 S1:1989 | Medical electrical equipment - Part 2: Particular requirements for the safety of electroconvulsive therapy equipment | Atcelts |
| 50700 | EN 60601-2-23:2000 | Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment | Atcelts |
| 51756 | HD 379 S1:1979 | Area exposure product meter | Atcelts |
| 48686 | EN 60601-1:1990/A11:1993 | Medical electrical equipment - Part 1: General requirements for safety | Atcelts |
| 55286 | LVS EN 80601-2-58:2009 | Medical electrical equipment - Part 2-58: Particular requirements for basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery (IEC 80601-2-58:2008) | Atcelts |
| 49052 | EN 60601-2-8:1997 | Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray equipment operating in the range 10 kV to 1 MV | Atcelts |
| 57964 | EN 60601-2-31:2008/A1:2011 | Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source | Atcelts |
| 43932 | EN 60601-2-45:2001 | Medical electrical equipment - Part 2-45: Particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices | Atcelts |
| 48076 | EN 80601-2-58:2009/A11:2011 | Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery | Atcelts |
| 51989 | 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 |
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