Logo
Login Sign Up
Current Revision

IEC 60601-2-23 Ed. 3.0 b:2011

Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment
Best Price Guarantee
Instant

$484.00

2-5 Days

$484.00

SAVE 10%

$871.20


Sub Total (1 Item(s))

$ 0.00

Estimated Shipping

$ 0.00

Total (Pre-Tax)

$ 0.00


or
International Electrotechnical Commission Logo

IEC 60601-2-23 Ed. 3.0 b:2011

Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment

PUBLISH DATE 2011
PAGES 100
IEC 60601-2-23 Ed. 3.0 b:2011
Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment
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.
SDO IEC: International Electrotechnical Commission
Document Number IEC 60601
Publication Date Feb. 1, 2011
Language b - English & French
Page Count 100
Revision Level 3.0
Supercedes
Committee 62d
Publish Date Document Id Type View
Feb. 1, 2011 IEC 60601-2-23 Ed. 3.0 b:2011 Revision
Feb. 1, 2011 Revision