Medical device licence · 71443 · Class 3
CENTRIMAG SYSTEM
Yes: licensed in Canada
Licence status Issued (active); first licensed May 25, 2006. It is in Health Canada’s list of active licences.
- Licence number
- 71443
- Licence holder
- Abbott MedicalPlymouth, MN, United States
- Risk class
- Class III (moderate to high risk)
- Licence type
- System
- First licensed
- May 25, 2006
- Devices covered
- 4
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- CENTRIMAG 2ND GEN PRIMARY CONSOLE
- CENTRIMAG BLOOD PUMP
- CENTRIMAG MOTOR
- CENTRIMAG RECHARGEABLE LI-ION BATTERY
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 “centrimag”. A notice may cover another product or only some lots: read it to see what it covers.
- CentriMag™ Adult ECMO Kit and Blood PumpOctober 22, 2025 · Cardiovascular - Gastroenterology and urology · Device compatibility - Performance · Type II
- 2nd Generation CentriMag™ Primary Console With Em-Tec Adult Flow ProbeJune 14, 2024 · Cardiovascular · Performance · Type II
- CentriMag Extracorporeal Blood Pumping System - Motor (2019-08-22)August 30, 2019 · Medical devices · Medical devices · Type II
- CentriMag Motor (2018-09-05)October 5, 2018 · Medical devices · Medical devices · Type I
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.