"ABBOTT" ARCHITECT i System (Non-Sterile)
Taiwan·Risk Class 1·MD·ABBOTT LABORATORIES·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- efdc1844e7a262a634bb9a0c6ab48235
- License Form
- Ministry of Health Medical Device Import Registration No. 019233
- Customs Code
- DHA08401923302
- 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)
- A2160 Individual photometric chemistry analyzer for clinical use
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
Top companies providing products similar to ""ABBOTT" ARCHITECT i System (Non-Sterile)"
Recently registered similar products
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.