Taiwan FDA registration 34ea8cf3e64522b6a227f49f5be8ac81
BECKMAN COULTER Synchron UniCel DxC 800 Clinical Systems (Non-Sterile)
TW: 貝克曼庫爾特協康 UniCel DxC800 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, 2026ActiveRegistration details
- Analysis ID
- 34ea8cf3e64522b6a227f49f5be8ac81
- License Form
- Ministry of Health Medical Device Import Registration No. 009565
- Customs Code
- DHA08400956505
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
- 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
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for BECKMAN COULTER Synchron UniCel DxC 800 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 34ea8cf3e64522b6a227f49f5be8ac81 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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