Medical device licence · 2149 · Class 2
FLO-RESTER SIZER
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed March 31, 1999; ended October 25, 2016. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 2149
- Licence holder
- Synovis Life Technologies, Inc. A Subsidiary Of Baxter International IncSt-Paul, MN, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Family
- First licensed
- March 31, 1999
- Ended
- October 25, 2016
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- FLO-RESTER SIZER PACK
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 “flo-rester”. A notice may cover another product or only some lots: read it to see what it covers.
- Baxter Flo-Thru, Flo-Rester and Vascular ProbeMarch 8, 2024 · Cardiovascular · Labelling and packaging · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.