Medical device licence · 7039 · Class 2
HBF QUIPLATE
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed July 5, 1999; ended November 1, 2012. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 7039
- Licence holder
- Helena Laboratories, CorpBeaumont, TX, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Test Kit
- First licensed
- July 5, 1999
- Ended
- November 1, 2012
- Devices covered
- 2
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- HBF QUIPLATE CONTROL
- HBF QUIPLATE PROCEDURE
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.