"Abbott" Designer Automatic Analyzer (without ICT module) (unsterilized)
Taiwan·Risk Class 1·ABBOTT LABORATORIES·Registered Feb 25, 2019 – Feb 25, 2024Cancelled- Analysis ID
- 1e98defcedb120142fe4205c900af49f
- Customs Code
- DHA09402012100
- 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
- Feb 25, 2019
- Expiry Date
- Feb 25, 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" Designer Automatic Analyzer (without ICT module) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1e98defcedb120142fe4205c900af49f 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, 1 companies making similar products including ABBOTT LABORATORIES, 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.