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EN 60601-2-49:2001 Standard

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  Keywords:

#specifies #collect #information #single #process

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipmentIEC 60601-2-49:2001

  Purpose

Specifies requirements for the safety of multifunction patient monitoring equipment. Multifunction patient monitoring equipment is defined as a modular or pre-configured device including more than one physiological monitoring unit designed to collect information from a single patient and process it for monitoring purposes and to generate alarms.

  Publication

Friday 17th of November 2017

  Related Standards

EN ISO 21534:2009

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EN 60601-2-26:2003

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Medical electrical equipment - Part 2-26: Particular requirements for the safety of electroencephalographsIEC 60601-2-26:2002

EN 60601-2-16:1998

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Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofil...

EN 60601-2-16:1998/AC:1999

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Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofil...

EN 60601-2-18:1996/A1:2000

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Medical electrical equipment - Part 2: Particular requirements for the safety of endoscopic equipmentIEC 60601-2-18:1996

EN 60601-2-23:2000

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Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneo...

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