Medical device licence · 64288 · Class 2
MULTIGENT - AEROSET/C8000 HEMOGLOBIN A1C
No longer licensed: cancelled
Licence status Cancelled; first licensed May 5, 2004; ended February 27, 2026. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 64288
- Licence holder
- Fisher Diagnostics, A Division Of Fisher Scientific Company, L.L.C.Middletown, VA, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Test Kit
- First licensed
- May 5, 2004
- Ended
- February 27, 2026
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- MULTIGENT - AEROSET/C8000 HEMOGLOBIN A1C KIT
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 “multigent”. A notice may cover another product or only some lots: read it to see what it covers.
- Multigent Creatinine (Enzymatic)July 6, 2017 · Medical devices · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.