Abbott clinical biochemical immunoglobulin A test group
- Analysis ID
- 5e0697e5fc03cb491386bb16af810d52
- Customs Code
- DHA00601782204
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- Immunoglobulin A can be quantitatively analyzed in human serum or plasma.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
- Import Information
- Contract manufacturing;; input
- Registration Date
- Dec 05, 2006
- Expiry Date
- Dec 05, 2026
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Access comprehensive regulatory information for Abbott clinical biochemical immunoglobulin A test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e0697e5fc03cb491386bb16af810d52 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.