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DIN EN 1642

Dentistry - Medical devices for dentistry - Dental implants

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Organization: DIN
Publication Date: 1 June 2012
Status: active
Page Count: 13
ICS Code (Dental implants): 11.060.15
scope:

This European Standard specifies general requirements for dental implants and accessories. Surgically implantable dental materials defined as restorative materials are specifically excluded and described in EN 1641.

This European Standard includes requirements for intended performance, design attributes, components, sterilization, packaging, marking, labelling, and information supplied by the manufacturer.

Document History

DIN EN 1642
June 1, 2012
Dentistry - Medical devices for dentistry - Dental implants
This European Standard specifies general requirements for dental implants and accessories. Surgically implantable dental materials defined as restorative materials are specifically excluded and...
DIN EN 1642
February 1, 2010
Dentistry - Medical devices for dentistry - Dental implants
A description is not available for this item.
DIN EN 1642
September 1, 2004
Dentistry - Medical devices for dentistry - Dental implants
A description is not available for this item.
DIN EN 1642
October 1, 1996
Medical devices for dentistry - Dental implants
A description is not available for this item.

References

This document references:
EN 1041 - Information supplied by the manufacturer of medical devices
Published by CEN on August 1, 2008
This European Standard specifies requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical...
This document references:
EN 21942-1 - Dental Vocabulary - Part 1: General and Clinical Terms
Published by CEN on August 1, 1991
A description is not available for this item.
This document references:
EN 21942-2 - Dental Vocabulary - Part 2: Dental Materials
Published by CEN on September 1, 1992
A description is not available for this item.
This document references:
EN 556-1 - Sterilization of Medical Devices - Requirements for Medical Devices to Be Designated "Sterile" - Part 1: Requirements for Terminally Sterilized Medical Devices
Published by CEN on October 1, 2001
This European Standard specifies the requirements for a terminally-sterilized medical device to be designated "STERILE". Part 2 of this European Standard specifies the requirements for an aseptically...
This document references:
EN 980 - Symbols for use in the labelling of medical devices
Published by CEN on May 1, 2008
This European Standard specifies symbols for use in the information supplied by the manufacturer with medical devices. The requirements of this European Standard are not intended to apply to symbols...
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