ApprovalTrail

Medical device licence · 92799 · Class 2

AQUILEX FLUID CONTROL SYSTEM

No longer licensed: suspended

Licence status Suspended; first licensed February 11, 2014; ended February 21, 2022. It is in Health Canada’s archive of licences no longer in force.
Licence number
92799
Licence holder
Hologic, Inc.Sunnyvale, CA, United States
Risk class
Class II (low to moderate risk)
Licence type
System
First licensed
February 11, 2014
Ended
February 21, 2022
Devices covered
10

Devices on this licence

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

  • AQUILEX FLUID CONTROL SYSTEM
  • AQUILEX FLUID CONTROL SYSTEM CANISTER KIT
  • AQUILEX FLUID CONTROL SYSTEM CANISTER RINGS (BEMIS)
  • AQUILEX FLUID CONTROL SYSTEM CART AND SCALE ASSEMBLY
  • AQUILEX FLUID CONTROL SYSTEM INFLOW TUBE
  • AQUILEX FLUID CONTROL SYSTEM OUTFLOW TUBE
  • AQUILEX FLUID CONTROL SYSTEM POWER CORD
  • AQUILEX FLUID CONTROL SYSTEM PUMP ASSEMBLY
  • AQUILEX FLUID CONTROL SYSTEM VACUUMTUBE
  • AQUILEX FLUID CONTROL SYSTEMS COMPLETE TUBE SET

Recalls and safety alerts that mention it

Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “aquilex”. A notice may cover another product or only some lots: read it to see what it covers.

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