Medical device licence · 859 · Class 2
BOTOX INJECTION NEEDLE
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed January 25, 1999; ended November 10, 2003. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 859
- Licence holder
- Allergan Sales, LlcIrvine, CA, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Single Device
- First licensed
- January 25, 1999
- Ended
- November 10, 2003
- Devices covered
- 1
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- BOTOX INJECTION NEEDLE
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 “botox”. A notice may cover another product or only some lots: read it to see what it covers.
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Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.