"Abbott" Designer Automatic Analyzer (without ICT module) (unsterilized) - Taiwan Registration 1e98defcedb120142fe4205c900af49f
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.
Device Details
Product Details
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.
A Clinical chemistry and clinical toxicology
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Input;; QMS/QSD
Dates and Status
Feb 25, 2019
Feb 25, 2024
Sep 30, 2021
Cancellation Information
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