This European Standard specifies general requirements for instruments used in the practice of dentistry and which are medical devices. It includes requirements for intended performance, design attributes, components, sterilization, packaging, marking, labelling, and information supplied by the manufacturer.
This European Standard does not apply to any necessary energy source to which an instrument needs to be connected. These energy sources are covered by the level 2 and level 3 standards, for dental equipment.
Tests for demonstrating compliance with this European Standard are contained in the level 3 standards, if appropriate.
Legislation related to this standard
WITHDRAWN
EN 1639:1996
WITHDRAWN
EN 1639:2004
99.60
Withdrawal effective
Oct 28, 2009
PUBLISHED
EN 1639:2009