ApprovalTrail

Medical device licence · 98248 · Class 3

LIMAX 120 LASER SYSTEM

No longer licensed: cancelled

Licence status Cancelled; first licensed December 16, 2016; ended May 3, 2022. It is in Health Canada’s archive of licences no longer in force.
Licence number
98248
Licence holder
Kls Martin L.P.Jacksonville, FL, United States
Risk class
Class III (moderate to high risk)
Licence type
System
First licensed
December 16, 2016
Ended
May 3, 2022
Devices covered
14

Devices on this licence

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

  • AUTOCLAVABLE FOCUSSING HAND PIECE
  • BARE FIBER
  • BARE FIBER 300 UM
  • BARE FIBER 400 UM
  • BARE FIBER 600 UM
  • ENDOTRACHEAL LASER INSTRUMENT
  • FIBER FOR HANDPIECE
  • FOCUSING HANDPIECE, LIMAX
  • GAS COOLED FIBER 400 UM
  • GAS-IRRIGATED FIBER
  • LIMAX 120
  • LIMAX 120 LASER SYSTEM
  • LINK FIBER
  • THORACOSCOPIC LASER INSTRUMENT

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