Medical device licence · 1183 · Class 2
RA-1000 ANALYZER SYSTEM
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed February 17, 1999; ended October 25, 2007. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 1183
- Licence holder
- Siemens Healthcare Diagnostics Inc.Newark, DE, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- System
- First licensed
- February 17, 1999
- Ended
- October 25, 2007
- Devices covered
- 25
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- RA-1000 ALBUMIN KIT
- RA-1000 ALERT 1
- RA-1000 ALERT 2
- RA-1000 ALKALINE PHOSPHATE KIT
- RA-1000 ALT KIT
- RA-1000 AMYLASE KIT
- RA-1000 ANALYZER
- RA-1000 AST KIT
- RA-1000 CALCIUM KIT
- RA-1000 CALIBRATOR
- RA-1000 CHOLESTEROL KIT
- RA-1000 CK KIT
- RA-1000 CREATININE KIT
- RA-1000 GGT KIT
- RA-1000 GLUCOSE HEXOKINASE KIT
- RA-1000 INORGANIC PHOSPHATE KIT
- RA-1000 LD KIT
- RA-1000 RANDOM ACCESS FLUID
- RA-1000 SERUM BLANK SOLUTION
- RA-1000 TOTAL BILIRUBIN KIT
- RA-1000 TOTAL PROTEIN KIT
- RA-1000 TRIGLYCERIDE KIT
- RA-1000 UREA NITROGEN KIT
- RA-1000 URIC ACID KIT
- RA-1000 WETTING AGENT
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.