Medical device licence · 6583 · Class 2
D-DIMER ASSAY KIT
No longer licensed: cancelled
Licence status Cancelled; first licensed June 28, 1999; ended June 25, 2013. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 6583
- 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
- June 28, 1999
- Ended
- June 25, 2013
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- THROMBOSCREEN D-DINER ASSAY KIT
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.