Apex complement C3 assay group
Taiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH·Registered Feb 13, 2019 – Feb 13, 2029Active- Analysis ID
- a403dd3e56d56a19a5a489ba42af67ae
- Customs Code
- DHA05603217302
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- This product quantifies Complement C3 in human serum or plasma on an Alinity c analyzer.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5240 補體成份免疫試驗系統
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Feb 13, 2019
- Expiry Date
- Feb 13, 2029
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Access comprehensive regulatory information for Apex complement C3 assay group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a403dd3e56d56a19a5a489ba42af67ae and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Made (部分製程) in JAPAN;; ABBOTT IRELAND DIAGNOSTICS DIVISION, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.