Medical device licence · 1251 · Class 2
560 EXPRESS PLUS CHEMISTRY ANALYZER
No longer licensed: discontinued at renewal
Licence status Discontinued at renewal; first licensed February 17, 1999; ended November 1, 2010. It is in Health Canada’s archive of licences no longer in force.
- Licence number
- 1251
- Licence holder
- Siemens Healthcare Diagnostics Inc.Newark, DE, United States
- Risk class
- Class II (low to moderate risk)
- Licence type
- Single Device
- First licensed
- February 17, 1999
- Ended
- November 1, 2010
- Devices covered
- 28
Devices on this licence
By name, as listed. The official record lists model numbers and identifiers.
- 560 EXPRESS PLUS
- ALBUMIN REAGENT
- ALKALINE PHOSPHATASE (IFCC) REAGENT
- ALT (IFCC) REAGENT
- AMMONIA REAGENT
- AMYLASE REAGENT
- AST REAGENT
- BUN REAGENT
- CALCIUM REAGENT
- CHLORIDE REAGENT
- CHOLESTEROL REAGENT
- CHOLINESTERASE REAGENT
- CREATININE KINASE (CK) REAGENT
- CREATININE REAGENT
- DIRECT BILIRUBIN REAGENT
- GAMMA-GT (IFCC) REAGENT
- GLUCOSE HK REAGENT
- GLUCOSE OXIDASE REAGENT
- HBD (HYDROXYBUTYRIC DEHYDROGENASE)
- HDL - CHOLESTEROL PRECIPITANT
- INORGANIC PHOSPHORUS REAGENT
- IRON REAGENT
- LDH-L REAGENT
- MAGNESIUM REAGENT (LIQUID)
- TOTAL BILIRUBIN REAGENT
- TOTAL PROTEIN REAGENT
- TRIGLYCERIDE REAGENT
- URIC ACID REAGENT
Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.