"ABBOTT" ARCHITECT i System (Non-Sterile)
Taiwan·Risk Class 1·MD·ABBOTT LABORATORIES·Registered Jun 25, 2018 – Jun 25, 2023Cancelled- Analysis ID
- 3aab9a1f738d1b911308aa6f53520275
- License Form
- Ministry of Health Medical Device Import No. 019233
- Customs Code
- DHA09401923308
- Manufacturer
- ABBOTT LABORATORIES
- Manufacturer Country
- United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
- 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
- Jun 25, 2018
- Expiry Date
- Jun 25, 2023
- Status
- Logged out
- Reason
- 轉為登錄字號
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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.