"Abbott" Designer Automated Immunoassay Analyzer (Unsterilized)
Taiwan·Risk Class 1·ABBOTT LABORATORIES·Registered Sep 26, 2020 – Sep 26, 2025Cancelled- Analysis ID
- ab28234c4b419222a3e667ae803a8b5d
- Customs Code
- DHA09402199205
- Manufacturer
- ABBOTT LABORATORIES
- Manufacturer Country
- United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Sep 26, 2020
- Expiry Date
- Sep 26, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Abbott" Designer Automated Immunoassay Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ab28234c4b419222a3e667ae803a8b5d and manufactured by ABBOTT LABORATORIES. 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 FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD, ABBOTT LABORATORIES, and 5 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.