ApprovalTrail

Medical device licence · 80389 · Class 2

RE-USABLE FOREIGN BODY RETRIEVERS

No longer licensed: discontinued at renewal

Licence status Discontinued at renewal; first licensed August 6, 2009; ended November 27, 2017. It is in Health Canada’s archive of licences no longer in force.
Licence number
80389
Licence holder
Endo-Flex GmbhVoerde, Germany
Risk class
Class II (low to moderate risk)
Licence type
Device Family
First licensed
August 6, 2009
Ended
November 27, 2017
Devices covered
13

Devices on this licence

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

  • FOREIGN BODY RETRIEVERS (RE-USABLE), 1.8 MM, GRASPERS, 3 PRONG
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 1.8 MM, GRASPERS, ALLIGATOR JAWS
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 1.8 MM, GRASPERS, CONI. ALLIGATOR JAWS
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 1.8 MM, GRASPERS, LONG ALLIGATOR JAWS
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 1.8 MM, GRASPERS, RAT TOOTH
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 1.8 MM, GRASPERS, TEETH
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 2.3 MM, GRASPERS, ALLIGATOR JAWS
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 2.3 MM, GRASPERS, CONI. ALLIGATOR JAWS
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 2.3 MM, GRASPERS, RAT TOOTH
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 2.3 MM, GRASPERS, TEETH
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 2.6 MM, GRASPERS, 3 PRONG
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 2.6 MM, GRASPERS, 4 PRONG
  • FOREIGN BODY RETRIEVERS (RE-USABLE), 2.6 MM, GRASPERS, 5 PRONG

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