"Abbott" Automated Immunoassay Analyzer (Unsterilized)
Taiwan·Risk Class 1·ABBOTT LABORATORIES·Registered Oct 01, 2019 – Oct 01, 2024Cancelled- Analysis ID
- 315cb14fadf70fdda4f0f8a6d1a1cca0
- Customs Code
- DHA09402090900
- 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
- Input;; QMS/QSD
- Registration Date
- Oct 01, 2019
- Expiry Date
- Oct 01, 2024
- 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" 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 315cb14fadf70fdda4f0f8a6d1a1cca0 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 ABBOTT LABORATORIES, SANMINA-SCI SYSTEMS SINGAPORE PTE LTD, 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.