ApprovalTrail

Medical device licence · 69006 · Class 2

INFILTRATION* CANNULA

No longer licensed: cancelled

Licence status Cancelled; first licensed August 9, 2005; ended June 12, 2013. It is in Health Canada’s archive of licences no longer in force.
Licence number
69006
Licence holder
Byron Medical Inc.Tucson, AZ, United States
Risk class
Class II (low to moderate risk)
Licence type
Device Family
First licensed
August 9, 2005
Ended
June 12, 2013
Devices covered
16

Devices on this licence

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

  • COLEM STYLE II W/"S" SHAPED CURVE CANNULA
  • COLEMAN INFILTRATION CANNULA STYLE I-BODY
  • COLEMAN INFILTRATION CANNULA STYLE II
  • COLEMAN INFILTRATION CANNULA STYLE III
  • COLEMAN INFITRATION CANNULA STYLE I
  • COLEMAN STYLE II W/CONCAVE CURVE CANNULA
  • COLEMAN STYLE MINI II
  • DONOFRIO INFILTRATION CANNULA
  • HUNSTAD INFILTRATION CANNULA
  • LAMIS INFILTRATION CANNULA
  • SIEMAN INFILTRATION CANNULA
  • VIDA MICROINJECTOR LUER LOCK BUTTERFLY CANNULA
  • VIDA MICROINJECTOR LUER LOCK BUTTERFLY FLATTENED CANNULA
  • VIDA MICROINJECTOR LUER LOCK CANNULA
  • VIDA MICROINJECTOR LUER LOCK FLATTENED CANNULA
  • VIDA MICROINJECTOR LUER LOCK NASAL CANNULA

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