Medical device licence · 87832 · Class 2
ANTISERA AND FIXATIVE KIT
No longer licensed: cancelled
Licence status Cancelled; first licensed December 12, 2011; ended May 13, 2014. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 87832
- Licence holder
- Interlab S.R.L.Roma, Italy
- Risk class
- Class II (low to moderate risk)
- Licence type
- Test Kit
- First licensed
- December 12, 2011
- Ended
- May 13, 2014
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- ANTISERA AND FIXATIVE 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 “antisera”. A notice may cover another product or only some lots: read it to see what it covers.
- Pneumococci Factor 7F Antisera (2018-11-19)January 8, 2019 · Medical devices · Medical devices · Type III
- E. Coli H Pool A-F Antisera (2014-01-15)April 7, 2014 · Medical devices · Medical devices · Type III
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.