Cimosir protein S reagent
Taiwan·Risk Class 2·INSTRUMENTATION LABORATORY CO.·Registered Jan 18, 2013 – Jan 18, 2028Active- Analysis ID
- 11c1945c49d777ca81fa9288b2d7b735
- Customs Code
- DHA00602432000
- Manufacturer
- INSTRUMENTATION LABORATORY CO.
- Manufacturer Country
- United States
- Authorized Representative
- Werfen Taiwan Limited
- Intended Use
- The concentration of protein S in human citrate acidated plasma was determined in the IL automatic coagulation instrument system (ACL TOP Family, ACL ELITE/ELITE PRO/8/9/1000, ACL Advance and ACL classic (100-7000)).
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.7290 factor deficiency test
- Import Information
- import
- Registration Date
- Jan 18, 2013
- Expiry Date
- Jan 18, 2028
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Access comprehensive regulatory information for Cimosir protein S reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 11c1945c49d777ca81fa9288b2d7b735 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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