Apex immunoglobulin M test set
Taiwan·Risk Class 2·ABBOTT IRELAND DIAGNOSTICS DIVISION·Registered Feb 11, 2022 – Feb 11, 2027Active- Analysis ID
- a1c6ed484b6c8e16039f188c657217e1
- Customs Code
- DHA05603521902
- Manufacturer
- ABBOTT IRELAND DIAGNOSTICS DIVISION
- Manufacturer Country
- Ireland
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- This product is used to quantify IgM in human serum or plasma on the Alinity c System.
- 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
- QMS/QSD;; 輸入
- Registration Date
- Feb 11, 2022
- Expiry Date
- Feb 11, 2027
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Access comprehensive regulatory information for Apex immunoglobulin M test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a1c6ed484b6c8e16039f188c657217e1 and manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. 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 FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH, 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.