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UNE-EN ISO 7494-1:2012

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

Dentistry - Dental units - Part 1: General requirements and test methods (ISO 7494-1:2011)
Available format(s)

Hardcopy , PDF

Superseded date

07-03-2019

Language(s)

Spanish, Castilian, English

Published date

02-15-2012

Committee
CTN 106
DocumentType
Standard
Pages
14
PublisherName
Asociacion Espanola de Normalizacion
Status
Superseded
SupersededBy
Supersedes

ISO 11226:2000 Ergonomics — Evaluation of static working postures
ISO 21530:2004 Dentistry — Materials used for dental equipment surfaces — Determination of resistance to chemical disinfectants
IEC 80601-2-60:2012 Medical electrical equipment - Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment
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ISO 4073:2009 Dentistry Information system on the location of dental equipment in the working area of the oral health care provider
ISO 6875:2011 Dentistry Patient chair
IEC 62366:2007+AMD1:2014 CSV Medical devices - Application of usability engineering to medical devices
IEC 62304:2006+AMD1:2015 CSV Medical device software - Software life cycle processes
ISO 1942:2009 Dentistry Vocabulary
ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
IEC 62353:2014 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
ISO 9687:2015 Dentistry Graphical symbols for dental equipment
ISO 11144:1995 Dental equipment Connections for supply and waste lines
ISO 6385:2016 Ergonomics principles in the design of work systems
IEC 60601-1-4:1996+AMD1:1999 CSV Medical electrical equipment - Part 1-4: General requirements for safety - Collateral Standard: Programmable electrical medical systems
ISO 17664:2017 Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices

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