Taiwan FDA registration 3f2098249194856f02f8b0c1547c4476
"Siemens" cholinesterase test reagent (unsterilized)
TW: "西門子" 膽鹼酯酶檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·SENTINEL CH. S.p.A.·Registered Jul 04, 2023 – Jul 04, 2028ActiveRegistration details
- Analysis ID
- 3f2098249194856f02f8b0c1547c4476
- Customs Code
- DHA09402317101
Company information
- Manufacturer
- SENTINEL CH. S.p.A.
- Manufacturer Country
- Italy
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "Bilister Enzyme Test System (A.3240)" first grade identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3240 Bile ester enzyme test system
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 04, 2023
- Expiry Date
- Jul 04, 2028
About this record
Access comprehensive regulatory information for "Siemens" cholinesterase test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f2098249194856f02f8b0c1547c4476 and manufactured by SENTINEL CH. S.p.A.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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