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This International Standard applies to the basic safety and essential performance of transcutaneous partial pressure monitoring equipment. This standard applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth. This standard does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa).
Author | VDE |
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Editor | VDE |
Document type | Standard |
Format | Paper |
ICS | 11.040.55 : Diagnostic equipment
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Number of pages | 56 |
Replace | DIN EN 60601-2-23 (2000-11) |
Cross references | EN 60601-2-23 (2015-10), IDT |
Weight(kg.) | 0.1952 |
Year | 2016 |
Document history | DIN EN 60601-2-23 (2016-08) |
Country | Germany |
Keyword | DIN EN 60601;DIN EN 60601-2;EN 60601;EN 60601-2;EN 60601-2-23;60601 |