Medical device licence · 9147 · Class 2
SPIFE ELECTROPHORESIS SYSTEM
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed July 29, 1999; ended October 21, 2011. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 9147
- Licence holder
- Helena Laboratories, CorpBeaumont, TX, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- System
- First licensed
- July 29, 1999
- Ended
- October 21, 2011
- Devices covered
- 14
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- SPIFE ELECTROPHORESIS SYSTEM - ACID HEMOGLOBIN
- SPIFE ELECTROPHORESIS SYSTEM - ALKALINE HB (HEMOGLOBIN) KIT
- SPIFE ELECTROPHORESIS SYSTEM - ALKALINE PHOSPHATASE ISOENZYME
- SPIFE ELECTROPHORESIS SYSTEM - ANALYZER
- SPIFE ELECTROPHORESIS SYSTEM - IMMUNOFIX KIT
- SPIFE ELECTROPHORESIS SYSTEM - LD ISOENZYME
- SPIFE ELECTROPHORESIS SYSTEM - LIPOPROTEIN
- SPIFE ELECTROPHORESIS SYSTEM - SPE HI RES KIT
- SPIFE ELECTROPHORESIS SYSTEM - SPE KIT
- SPIFE ELECTROPHORESIS SYSTEM - SPE VIS KIT
- SPIFE ELECTROPHORESIS SYSTEM - SPLIT BETA SPE
- SPIFE ELECTROPHORESIS SYSTEM - ULTRA IMMUNOFIX
- SPIFE ELECTROPHORESIS SYSTEM - VIS CHOLESTEROL PROFILE
- STOPCOCK MANIFOLD
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.