Medical device licence · 73139 · Class 2
FLOSEAL ENDOSCOPIC APPLICATOR
No longer licensed: cancelled
Licence status Cancelled; first licensed January 22, 2007; ended January 28, 2015. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 73139
- Licence holder
- Baxter Healthcare CorporationDeerfield, Illinois, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Group
- First licensed
- January 22, 2007
- Ended
- January 28, 2015
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- FLOSEAL ENDOSCOPIC APPLICATOR
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 “floseal”. A notice may cover another product or only some lots: read it to see what it covers.
- Coseal Premix Surgical Sealant, Floseal Hemostatic Matrix & Hemopatch Bicarb (2019-09-23)October 25, 2019 · Medical devices · Medical devices · Type III
- Floseal Hemostatic Matrix (2013-11-12)January 6, 2014 · Medical devices · Medical devices · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.