ApprovalTrail

Medical device licence · 70172 · Class 3

PERIFLUX SYSTEM 5000

No longer licensed: discontinued at renewal

Licence status Discontinued at renewal; first licensed January 11, 2006; ended October 31, 2018. It is in Health Canada’s archive of licences no longer in force.
Licence number
70172
Licence holder
Perimed AbJarfalla, Sweden
Risk class
Class III (moderate to high risk)
Licence type
System
First licensed
January 11, 2006
Ended
October 31, 2018
Devices covered
15

Devices on this licence

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

  • PERIFLUX SYSTEM 5000 - A/D CONVERTER
  • PERIFLUX SYSTEM 5000 - CALIBRATION DEVICE
  • PERIFLUX SYSTEM 5000 - ELECTRODE HOLDER
  • PERIFLUX SYSTEM 5000 - ELECTRODE HOLDER KIT
  • PERIFLUX SYSTEM 5000 - PERISOFT FOR WINDOWS
  • PERIFLUX SYSTEM 5000 - PF 5001 MAIN UNIT
  • PERIFLUX SYSTEM 5000 - PF 5002 BASIC MAIN UNIT
  • PERIFLUX SYSTEM 5000 - PF 5010 LDPM UNIT
  • PERIFLUX SYSTEM 5000 - PF 5020 HEAT UNIT
  • PERIFLUX SYSTEM 5000 - PF 5040 RC TCPO2/TCPCO2 UNIT
  • PERIFLUX SYSTEM 5000 - PF 5040 TCPO2/TCPCO2 UNIT
  • PERIFLUX SYSTEM 5000 - PF 5050 PRESSURE UNIT
  • PERIFLUX SYSTEM 5000 - PROBE HOLDERS
  • PERIFLUX SYSTEM 5000 - PROBES
  • PERIFLUX SYSTEM 5000 - REMOTE PANELS

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