| Reference |
IEC 60601-2-23 ed3.0 withdrawn corrigendum |
> preview
|
| Title |
Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment
|
| Publication date |
2011-02-25 |
Format, price
(Swiss francs)
and language |
 | 230.- |
| 95 pages |  | 230.- |
| 1617 Kb |
|
| |
| Abstract |
IEC 60601-2-23:2011 applies to the basic safety and essential performance of transcutaneous partial pressure monitoring equipment. It applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth. IEC 60601-2-23:2011 does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa).
This third edition cancels and replaces the second edition published in 1999 and constitutes a technical revision. This edition of IEC 60601-2-23 was revised to align structurally with the 2005 edition of IEC 60601-1.
|
| Technical Committee |
62D - Electromedical equipment
|
| ICS Codes |
| 11.040.55 |
Diagnostic equipment
*Including medical monitoring equipment, medical thermometers and related materials |
|
| |
| Replaced by |
|
| Stability date |
2015 |
| |
| Work in progress |
| Project | Stage code | Forecast publication date |
|---|
| No project under development | - | - |
|
Search
Quick access by ref. number
Basket
Payment
Just Published
Bestsellers