Medical electrical equipment Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

11-30-2015

Publisher

British Standards Institution

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.

Committee	CH/62/4
DevelopmentNote	Supersedes BS EN 60601-3.1. (05/2000) Supersedes and renumbers BS 5724-2.123(1996) (07/2004) Supersedes BS 5724-3.101(1997). (08/2015) 2000 Edition remains active & will be withdrawn on 15/09/2018. Supersedes 09/30172484 DC. (11/2015)
DocumentType	Standard
Pages	54
PublisherName	British Standards Institution
Status	Current
Supersedes	BS 5724-3.101(1997) : 1997 BS 5724-2.123(1996) : AMD 10042 09/30172484 DC : 0 BS EN 60601-2-23:2000 BS EN 60601-3-1:1997

Standards	Relationship
IEC 60601-2-23:2011	Identical
I.S. EN 60601-2-23:2015	Identical
SN EN 60601-2-23 : 2000	Identical
DIN EN 60601-2-23 : 2016	Identical
EN 60601-2-23:2015	Identical
NF EN 60601-2-23 : 2016	Identical
UNE-EN 60601-2-23:2001	Identical
EN 61966-6:2006	Identical

EN 60601-2-49:2015	Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment
IEC 60601-1-8:2006+AMD1:2012 CSV	Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems
IEC 60601-1-2:2014	Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
EN 60601-1-2:2015	Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
IEC 60601-2-49:2011	Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment
EN 60601-1-8:2007/A11:2017	MEDICAL ELECTRICAL EQUIPMENT - PART 1-8: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: GENERAL REQUIREMENTS, TESTS AND GUIDANCE FOR ALARM SYSTEMS IN MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS (IEC 60601-1-8:2006/A1:2012)