Medical device licence · 2295 · Class 2
RAPID DRUG SCREEN
No longer licensed: cancelled: quality-system requirement (2003)
Licence status Cancelled: quality-system requirement (2003); first licensed April 13, 1999; ended February 16, 2004. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 2295
- Licence holder
- American Bio Medica CorporationKinderhook, NY, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Group Family
- First licensed
- April 13, 1999
- Ended
- February 16, 2004
- Devices covered
- 5
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- RAPID DRUG SCREEN 1-PANEL (SINGLE)
- RAPID DRUG SCREEN 3-PANEL
- RAPID DRUG SCREEN 5 PANEL
- RAPID DRUG SCREEN 8 PANEL
- RAPID DRUG SCREEN 9 PANEL
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.