I.S. EN ISO 6875:2011
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
DENTISTRY - PATIENT CHAIR
Hardcopy , PDF
01-31-2019
English
07-15-2011
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Classification
5 Requirements
6 Sampling
7 Testing
8 Manufacturer's information
9 Marking
10 Packaging
Bibliography
Pertains to all patient chairs, regardless of their construction, and regardless of whether they are operated manually, electrically or by other means, or as a combination of these.
| DocumentType |
Standard
|
| Pages |
21
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Withdrawn
|
| Supersedes |
| Standards | Relationship |
| SN EN ISO 6875 : 2011 | Identical |
| BS EN ISO 6875:2011 | Identical |
| NBN EN ISO 6875 : 2011 | Identical |
| DIN EN ISO 6875:2011-10 | Identical |
| EN ISO 6875:2011 | Identical |
| UNI EN ISO 6875 : 2011 | Identical |
| NS EN ISO 6875 : 2011 | Identical |
| NEN EN ISO 6875 : 2011 | Identical |
| NF EN ISO 6875 : 2011 | Identical |
| UNE-EN ISO 6875:2012 | Identical |
| ISO 6875:2011 | Identical |
| 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 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| ISO 4073:2009 | Dentistry Information system on the location of dental equipment in the working area of the oral health care provider |
| 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 8191-1:1987 | Furniture — Assessment of the ignitability of upholstered furniture — Part 1: Ignition source: smouldering cigarette |
| 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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