Taiwan FDA registration 32b304d7f4adcfd8c4081830a7a529cb
BECKMAN COULTER COULTER DxH Retic Pack (non-sterile)
TW: 貝克曼庫爾特庫爾特DxH 網狀紅血球處理劑(未滅菌)
Taiwan·Risk Class 1·MD·BECKMAN COULTER INC.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 32b304d7f4adcfd8c4081830a7a529cb
- License Form
- Ministry of Health Medical Device Import Registration No. 008376
- Customs Code
- DHA08400837600
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 grade identification range of dyes and chemical solution dyes (B.1850) of the management measures for medical devices.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B1850 Dyes and chemical solution dyes
- 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 COULTER DxH Retic Pack (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 32b304d7f4adcfd8c4081830a7a529cb 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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