Medical device licence · 13483 · Class 2
LATEX EXAMINATION GLOVES
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed October 28, 1999; ended October 29, 2021. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 13483
- Licence holder
- Maxill Inc.St. Thomas, Ontario, Canada
- Risk class
- Class II (low to moderate risk)
- Licence type
- Device Family
- First licensed
- October 28, 1999
- Ended
- October 29, 2021
- Devices covered
- 11
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- CRANBERRY CYNTEK POWDER FREE LATEX MEDICAL EXAMINATION GLOVE
- CRANBERRY SILKCARE FITTED POWDER FREE LATEX MEDICAL EXAMINATION GLOVE
- CRANBERRY SILKCARE POWDER FREE LATEX MEDICAL EXAMINATION GLOVE
- DERMEX LATEX PLATINUM POWDER FREE LATX MEDICAL EXAMINATION GLOVE
- DERMEX LATEX-LP LIGHTLY POWDERED LATEX MEDICAL EXAMINATION GLOVE
- DERMEX LATEX-PF POWDER FREE LATEX MEDICAL EXAMINATION GLOVE
- LATEX EXAMINATION GLOVES
- MAXILL LIGHTLY POWDERED LATEX MEDICAL EXAMINATION GLOVE
- MAXILL NATURAL RUBBER LATEX GLOVES
- MAXILL POWDER FREE LATEX MEDICAL EXAMINATION GLOVE
- PFL1 POWDER FREE LATEX EXAMINATION GLOVE
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.