CR 14060:2000

Medical device traceability CR 14060:2000

General information

99.60 Withdrawal effective   Dec 3, 2014

CEN/CENELEC

CEN/CLC/JTC 3 Quality management and corresponding general aspects for medical devices

CEN Report

11.040.01   Medical equipment in general

Scope

This technical report provides recommendations for procedures that should be followed to establish, as far as possible, a traceability route for medical devices which have been placed on the market.
It is understood that the procedures to be described in this report will be more detailed in relation to high-risk devices when the need has been identified to trace devices as far as the actual patient.

For lower risk devices this report provides recommendations for elements of procedures to be transmitted by manufacturers to the members of a distribution chain, to achieve an appropriate level of traceability, perhaps of batches of products in some cases, sufficient to withdraw or inform purchasers or users of information regarding such identified products.

Related legislation

Legislation related to this standard

90/385/EEC

Active implantable medical devices

93/42/EEC

Medical devices

Life cycle

NOW

WITHDRAWN
CR 14060:2000
99.60 Withdrawal effective
Dec 3, 2014

REVISED BY

WITHDRAWN
CEN/CLC/TR 14060:2014