EN 60601-3-1:1996
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Medical electrical equipment - Part 3-1: Essential performance requirements for transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment
01-07-1997
16-12-1996
Specifies essential requirements for the performance of transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment. Applies to transcutaneous monitors intended for use with adults, children and neonates, and includes the use of these devices in foetal monitoring during birth. Does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin such as conjunctiva or mucosa.
| Committee |
CLC/TC 62
|
| DocumentType |
Standard
|
| PublisherName |
European Committee for Standards - Electrical
|
| Status |
Withdrawn
|
| Standards | Relationship |
| IEC 60601-3-1:1996 | Identical |
| NBN EN 60601 3-1 : 1997 | Identical |
| NF EN 60601-3-1 : 2002 | Identical |
| I.S. EN 60601-3-1:1998 | Identical |
| PN EN 60601-3-1 : 2002 | Identical |
| SN EN 60601-3-1 : 1996 | Identical |
| UNE-EN 60601-3-1:1997 | Identical |
| BS EN 60601-3-1:1997 | Identical |
| BS 5724-3.101(1997) : 1997 | Identical |
| CEI EN 60601-3-1 : 1997 | Identical |
| DIN EN 60601-3-1:1998-11 | Identical |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| IEC 60601-2-23:2011 | Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment |
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