Taiwan FDA registration fb3e1b0b171e5674f5fc053aeb1ac27d
Cimosir Weberlander factor ristomycin cofactor active reagent
TW: 希摩西爾魏伯蘭特氏因子瑞斯托菌素輔因子活性試劑
Taiwan·Risk Class 2·INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.·Registered Dec 14, 2018 – Dec 14, 2028ActiveRegistration details
- Analysis ID
- fb3e1b0b171e5674f5fc053aeb1ac27d
- Customs Code
- DHA05603196402
Company information
- Manufacturer
- INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.
- Manufacturer Country
- Spain;;United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- This product is used with ACL TOP series instruments to automatically determine the concentration of Weberlander's factor ristomycin cofactor activity in human citrate acidified plasma.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7290 factor deficiency test
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Dec 14, 2018
- Expiry Date
- Dec 14, 2028
About this record
Access comprehensive regulatory information for Cimosir Weberlander factor ristomycin cofactor active reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb3e1b0b171e5674f5fc053aeb1ac27d and manufactured by INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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