BS EN 60601-2-23:2015
Current
The latest, up-to-date edition.
Medical electrical equipment Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment
Hardcopy , PDF
English
30-11-2015
Important note : Users cannot be edited or removed once added to your Multi user PDF.| Committee |
CH/62/4
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| 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 (08/2015) 2000 Edition remains active & will be withdrawn on 15/09/2018.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)
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| DocumentType |
Standard
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| Pages |
54
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| PublisherName |
British Standards Institution
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| Status |
Current
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| Supersedes |
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.
| 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) |
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