"ABBOTT" ARCHITECT i System (Non-Sterile) - Taiwan Registration 3aab9a1f738d1b911308aa6f53520275
Access comprehensive regulatory information for "ABBOTT" ARCHITECT i System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3aab9a1f738d1b911308aa6f53520275 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
Registration Details
3aab9a1f738d1b911308aa6f53520275
Ministry of Health Medical Device Import No. 019233
DHA09401923308
Product Details
A Clinical chemistry and clinical toxicology
A2160 Individual photometric chemistry analyzer for clinical use
Imported from abroad
Dates and Status
Jun 25, 2018
Jun 25, 2023
Cancellation Information
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