Medical device licence · 14917 · Class 4
HANCOCK PATCH PERICARDIAL
No longer licensed: cancelled
Licence status Cancelled; first licensed November 29, 1999; ended April 20, 2009. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 14917
- Licence holder
- Medtronic Inc.Minneapolis, MN, United States
- Risk class
- Class IV (highest risk)
- Licence type
- Single Device
- First licensed
- November 29, 1999
- Ended
- April 20, 2009
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- HANCOCK PATCH PERICARDIAL
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 “hancock”. A notice may cover another product or only some lots: read it to see what it covers.
- Mosaic/Hancock II Ultra Supra Sizer and Mosaic Obturator (2014-01-10)March 18, 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.