Taiwan FDA registration e379d4ec4ef0b1733836672064c20bc2
Cimosir Brandt factor antigen reagent
TW: 希摩西爾魏白蘭特因子抗原試劑
Taiwan·Risk Class 2·INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.·Registered Nov 21, 2005 – Nov 21, 2025ExpiredRegistration details
- Analysis ID
- e379d4ec4ef0b1733836672064c20bc2
- Customs Code
- DHA00601484300
Company information
- Manufacturer
- INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.
- Manufacturer Country
- Spain;;United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- The IL Blood Coagulation Instrument System quantifies the antigen concentration of Weiberante factor (VWF: Ag) in citrate acidified plasma using latex immunoassay.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7290 factor deficiency test
- Import Information
- import
Dates and status
- Registration Date
- Nov 21, 2005
- Expiry Date
- Nov 21, 2025
About this record
Access comprehensive regulatory information for Cimosir Brandt factor antigen reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e379d4ec4ef0b1733836672064c20bc2 and manufactured by INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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