EN ISO 9173-1:2016
Current
Current
The latest, up-to-date edition.
Dentistry - Extraction forceps - Part 1: General requirements (ISO 9173-1:2016)
Published date
30-11-2016
Publisher
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European foreword
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
5 Test methods
6 Marking
Bibliography
ISO 9173-1:2016 specifies the general performance requirements for extraction forceps used in dentistry.
| Committee |
CEN/TC 55
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Standards | Relationship |
| DIN EN ISO 9173-1:2017-03 | Identical |
| ISO 9173-1:2016 | Identical |
| PN EN ISO 9173-1 : 2017 | Identical |
| NEN EN ISO 9173-1 : 2016 | Identical |
| NF EN ISO 9173-1 : 2017 | Identical |
| I.S. EN ISO 9173-1:2016 | Identical |
| BS EN ISO 9173-1:2016 | Identical |
| NBN EN ISO 9173-1 : 2006 | Identical |
| DIN EN ISO 9173-1:2015-02 (Draft) | Identical |
| NS EN ISO 9173-1 : 2016 | Identical |
| UNE-EN ISO 9173-1:2016 | Identical |
| UNE-EN ISO 9173-1:2007 | Identical |
| 02/563808 DC : DRAFT SEP 2002 | BS EN 1639 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS |
| DIN EN 1639:2010-02 | Dentistry - Medical devices for dentistry - Instruments |
| BS EN 1639:2009 | Dentistry. Medical devices for dentistry. Instruments |
| I.S. EN 1639:2009 | DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS |
| 08/30184602 DC : DRAFT SEP 2008 | BS EN 1639 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS |
| EN 1639:2009 | Dentistry - Medical devices for dentistry - Instruments |
| ISO 9173-2:2010 | Dentistry — Extraction forceps — Part 2: Designation |
| ISO 6508-2:2015 | Metallic materials — Rockwell hardness test — Part 2: Verification and calibration of testing machines and indenters |
| ISO 1942:2009 | Dentistry — Vocabulary |
| ISO 7153-1:2016 | Surgical instruments — Materials — Part 1: Metals |
| ISO 9173-3:2014 | Dentistry — Extraction forceps — Part 3: Design |
| 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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