Medical device licence · 16342 · Class 4
DUODERM CGF BORDER DRESSING
Yes: licensed in Canada
Licence status Issued (active); first licensed January 24, 2000. It is in Health Canada’s list of active licences.
- Licence number
- 16342
- Licence holder
- Convatec Inc.Greensboro, NC, United States
- Risk class
- Class IV (highest risk)
- Licence type
- Single Device
- First licensed
- January 24, 2000
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- DUODERM CGF BORDER DRESSING
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 “duoderm”. A notice may cover another product or only some lots: read it to see what it covers.
- DuoDerm Sealing defect (2021-08-20)May 4, 2022 · General hospital and personal use · Labelling and packaging · Type II
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.