ApprovalTrail

Medical device licence · 24322 · Class 3

ALPHA-BSM-GENTA BONE SUBSTITUTE MATERIAL

No longer licensed: cancelled

Licence status Cancelled; first licensed October 24, 2000; ended December 1, 2020. It is in Health Canada’s archive of licences no longer in force.
Licence number
24322
Licence holder
Etex Corporation Adba Zimmer EtexBraintree, MA, United States
Risk class
Class III (moderate to high risk)
Licence type
Single Device
First licensed
October 24, 2000
Ended
December 1, 2020
Devices covered
1

Devices on this licence

By name, as listed. The official record lists model numbers and identifiers.

  • ALPHA-BSM-GENTA BONE SUBSTITUTE MATERIAL

Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.