Taiwan FDA registration 4a6e251bd414f4674bef5924ab4b4728
Cimosir Weberland factor quality control fluid
TW: 希摩西爾魏伯蘭特因子品管液
Taiwan·Risk Class 2·INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.·Registered Nov 03, 2022 – Nov 03, 2027ActiveRegistration details
- Analysis ID
- 4a6e251bd414f4674bef5924ab4b4728
- Customs Code
- DHA05603587800
Company information
- Manufacturer
- INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.
- Manufacturer Country
- Spain;;United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- Quality control monitoring of Weberland factor lyase activity reagents is performed on Bio-Flash.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.5425 Versatile system for in vitro agglutination studies
- Import Information
- 輸入;; QMS/QSD;; 委託製造
Dates and status
- Registration Date
- Nov 03, 2022
- Expiry Date
- Nov 03, 2027
About this record
Access comprehensive regulatory information for Cimosir Weberland factor quality control fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4a6e251bd414f4674bef5924ab4b4728 and manufactured by INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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