BS EN 60601-2-23:2000
Medical electrical equipment - Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment

Standard No.

BS EN 60601-2-23:2000

Release Date

2000

Published By

British Standards Institution (BSI)

Status

Be replaced 2015-11

Replace By

BS EN 60601-2-23:2015

Latest

BS EN 60601-2-23:2015

Replace

97/560871 DC-1997 BS EN 60601-2-23:1996 BS EN 60601-3-1:1997

Scope

Addition: This Particular Standard specifies requirements for the safety, including essential performance, of TRANSCUTANEOUS PARTIAL PRESSURE MONITORING EQUIPMENT, as defined in 2.101 and hereinafter referred to as EQUIPMENT, whether this EQUIPMENT is stand alone or part of a system. It applies to transcutaneous monitors used with adults, children and neonates, and it includes the use of these devices in foetal monitoring during birth. It does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin (for example conjunctiva, mucosa).

BS EN 60601-2-23:2000 history

• 2015 BS EN 60601-2-23:2015 Medical electrical equipment. Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment
• 2000 BS EN 60601-2-23:2000 Medical electrical equipment - Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment