Taiwan FDA registration be61b87924d0fdd5f086674e9b93e66e
BECKMAN COULTER SYNCHRON UniCel DxC Clinical Systems （Non-Sterile）
TW: 貝克曼庫爾特 協康(UniCel DxC)自動生化分析系統（未滅菌）
Taiwan·Risk Class 1·MD·BECKMAN COULTER INC.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- be61b87924d0fdd5f086674e9b93e66e
- License Form
- Ministry of Health Medical Device Import Registration No. 000610
- Customs Code
- DHA08400061004
Company information
- Manufacturer
- BECKMAN COULTER INC.
- Manufacturer Country
- United States
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- An instrument for clinical laboratories to perform automated qualitative/quantitative analysis of biochemical in vitro diagnostics.
- 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for BECKMAN COULTER SYNCHRON UniCel DxC Clinical Systems （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 be61b87924d0fdd5f086674e9b93e66e and manufactured by BECKMAN COULTER INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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