Abbott designer corticosterone test panel
Taiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT IRELAND DIAGNOSTICS DIVISION·Registered Apr 30, 2009 – Apr 30, 2029Active- Analysis ID
- ea009e71ff5d00b95ba0f8e6c9d76c1b
- Customs Code
- DHA00602000001
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- This product is used for the quantitative detection of corticosterone (cortisol) in human serum, plasma, or urine by chemical cold light microparticle immunoassay (CMIA) on the ARCHITECT i system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1205 皮質醇(氫基腎上腺素,及羥皮質固醇)試驗系統;; A.1150 校正品
- Import Information
- Contract manufacturing;; input
- Registration Date
- Apr 30, 2009
- Expiry Date
- Apr 30, 2029
Access comprehensive regulatory information for Abbott designer corticosterone test panel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea009e71ff5d00b95ba0f8e6c9d76c1b 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. 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.