"ABBOTT" ARCHITECT i System (Non-Sterile) - Taiwan Registration efdc1844e7a262a634bb9a0c6ab48235
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 efdc1844e7a262a634bb9a0c6ab48235 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
efdc1844e7a262a634bb9a0c6ab48235
Ministry of Health Medical Device Import Registration No. 019233
DHA08401923302
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
A2160 Individual photometric chemistry analyzer for clinical use
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2023