Api myoglobin test set
- Analysis ID
- efc182d750cdf2c41ecb01b9ed097f17
- Customs Code
- DHA05603350503
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- This product is used to quantitatively detect myoglobin in human serum and plasma by chemical cold light particle immunoassay (CMIA) on the Alinity i analyzer.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5680 肌紅蛋白免疫試驗系統
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Jul 14, 2020
- Expiry Date
- Jul 14, 2025
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Access comprehensive regulatory information for Api myoglobin 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 efc182d750cdf2c41ecb01b9ed097f17 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; 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, 2 companies making similar products including BIOKIT, S.A., FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT IRELAND DIAGNOSTICS DIVISION, and 2 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.