NA 022
DKE German Commission for Electrical, Electronic & Information Technologies of DIN and VDE
DIN EN 60335-2-8 ; VDE 0700-8:1996-06 [Withdrawn] references following documents:
| Document number | Edition | Title |
|---|---|---|
| EN 60601-2-25 | 1995-11 | Medical electrical equipment - Part 2: Particular requirements for the safety of electrocardiographs (IEC 60601-2-25:1993) More |
| EN 60601-2-26 | 1994-08 | Medical electrical equipment - Part 2: Particular requirements for the safety of electroencephalographs (IEC 60601-2-26:1994) More |
| EN 60601-2-27 | 1994-08 | Medical electrical equipment - Part 2: Particular requirements for the safety of electrocardiographic monitoring equipment (IEC 60601-2-27:1994) More |
| EN 60601-2-28 | 1993-05 | Medical electrical equipment; part 2: particular requirements for the safety of X-ray source assemblies and X-ray tube assemblies for medical diagnosis (IEC 60601-2-28:1993) More |
| EN 60601-2-29 | 1995-11 | Medical electrical equipment - Part 2: Particular requirements for the safety of radiotherapy simulators (IEC 60601-2-29:1993) More |
| EN 60601-2-3 | 1993-04 | Medical electrical equipment; part 2: particular requirements for the safety of short-wave therapy equipment (IEC 60601-2-3:1991) More |
| EN 60601-2-30 | 1995-07 | Medical electrical equipment - Part 2: Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment (IEC 60601-2-30:1995) More |
| EN 60601-2-31 | 1995-01 | Medical electrical equipment - Part 2: Particular requirements for the safety of external cardiac pacemakers with internal power source (IEC 60601-2-31:1994) More |
| EN 60601-2-32 | 1994-07 | Medical electrical equipment - Part 2: Particular requirements for the safety of associated equipment of X-ray equipment (IEC 60601-2-32:1994) More |
| EN 60601-2-33 | 1995-11 | Medical electrical equipment - Part 2: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:1995) More |
