Medical device licence · 73576 · Class 2
REMIPACK
No longer licensed: cancelled
Licence status Cancelled; first licensed March 14, 2007; ended June 13, 2018. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 73576
- Licence holder
- Janssen Inc.Toronto, Ontario, Canada
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Family
- First licensed
- March 14, 2007
- Ended
- June 13, 2018
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- REMIPACK
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 “remipack”. A notice may cover another product or only some lots: read it to see what it covers.
- Remipack (2018-03-28)April 6, 2018 · Medical devices · Medical devices · Type I
- Remipack (2013-12-12)February 3, 2014 · 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.