Abbott Designer Plus Analyzer - Taiwan Registration 1760bb2d3160a79bee12e87b7de6578d
Access comprehensive regulatory information for Abbott Designer Plus Analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1760bb2d3160a79bee12e87b7de6578d 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. 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 enzyme analyzer for clinical use (A.2500) of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A.2500 Enzyme analyzer for clinical use
import
Dates and Status
Jun 07, 2010
Jun 07, 2015
Aug 09, 2018
Cancellation Information
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