Taiwan FDA registration 8e30564939d12fcf405c83e06c7d7eb9
“Abbott”Alinity s system
TW: “亞培”自動免疫分析儀
Taiwan·Risk Class 2·MD·ABBOTT LABORATORIES·Registered Jul 05, 2019 – Jul 05, 2024ExpiredRegistration details
- Analysis ID
- 8e30564939d12fcf405c83e06c7d7eb9
- License Form
- Ministry of Health Medical Device Import No. 032461
- Customs Code
- DHA05603246104
Company information
- Manufacturer
- ABBOTT LABORATORIES
- Manufacturer Country
- United States
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- This product is a high-throughput, fully automated immunoassay analyzer that uses chemiluminescence immunoassay technology to determine specific antigens and antibodies.
- 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
Dates and status
- Registration Date
- Jul 05, 2019
- Expiry Date
- Jul 05, 2024
About this record
Access comprehensive regulatory information for “Abbott”Alinity s system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8e30564939d12fcf405c83e06c7d7eb9 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.
Free DatabasePowered by Pure Global AI89,000+ Devices