Taiwan FDA registration 265f38b4ec650a39798d2e4b9ca54b6a
“Beckman Coulter” DxFLEX Sheath Fluid (Non-Sterile)
TW: “貝克曼庫爾特” 締斯弗雷克斯鞘液溶液 (未滅菌)
Taiwan·Risk Class 1·MD·BECKMAN COULTER INC.·Registered Jun 22, 2020 – Jun 22, 2025ExpiredRegistration details
- Analysis ID
- 265f38b4ec650a39798d2e4b9ca54b6a
- License Form
- Ministry of Health Medical Device Import No. 021651
- Customs Code
- DHA09402165105
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 blood cell thinners (B.8200) of the management methods for medical devices.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B8200 Blood cell thinner
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 22, 2020
- Expiry Date
- Jun 22, 2025
About this record
Access comprehensive regulatory information for “Beckman Coulter” DxFLEX Sheath Fluid (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 265f38b4ec650a39798d2e4b9ca54b6a 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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