Medical device licence · 9432 · Class 2
AUTOVAC BLOOD PROCESSING SYSTEM
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed August 6, 1999; ended October 15, 2004. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 9432
- Licence holder
- Boehringer Laboratories, LlcPhoenixville, PA, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Group Family
- First licensed
- August 6, 1999
- Ended
- October 15, 2004
- Devices covered
- 6
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- AUTOVAC BP BLOOD PROCESSING SYSTEM
- AUTOVAC INTRAOPERATIVE AUTOTRANSFUSION SYSTEM
- AUTOVAC POSTOPERATIVE AUTOTRANSFUSION SYSTEM W/AUTOWICK
- AUTOVAC POSTOPERATIVE AUTOTRANSFUSION SYSTEM W/REGULATOR
- AUTOVAC SYSTEM MANIFOLD
- AUTOVAC TC POSTOPERATIVE AUTOTRANSFUSION SYSTEM W/AUTOWICK
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 “autovac”. A notice may cover another product or only some lots: read it to see what it covers.
- Autovac Biopsy Needle (2018-11-04)November 28, 2018 · 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.