Taiwan FDA registration b4ca5c81b704600f77b032479fa6c5ec
"Siemens Atellica" Cholinesterase Test (Non-Sterile)
TW: "西門子" 膽素酯酵素試劑 (未滅菌)
Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LIMITED·Registered Nov 14, 2017 – Nov 14, 2027ActiveRegistration details
- Analysis ID
- b4ca5c81b704600f77b032479fa6c5ec
- License Form
- Ministry of Health Medical Device Import No. 018497
- Customs Code
- DHA09401849701
Company information
- Manufacturer
- RANDOX LABORATORIES LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the bilisterase test system (A.3240) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A3240 Bilisterase Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 14, 2017
- Expiry Date
- Nov 14, 2027
About this record
Access comprehensive regulatory information for "Siemens Atellica" Cholinesterase Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b4ca5c81b704600f77b032479fa6c5ec and manufactured by RANDOX LABORATORIES LIMITED. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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