Taiwan FDA registration a0d2be1b70f652ea38007be6ce779045
Beckman Coulter Human Growth Hormone Reagent Set (non-sterile)
TW: 貝克曼庫爾特人類生長激素試劑組(未滅菌)
Taiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered Sep 10, 2024 – Sep 10, 2029ActiveRegistration details
- Analysis ID
- a0d2be1b70f652ea38007be6ce779045
- Customs Code
- DHA09402360001
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
- It is limited to the first level of identification of the human growth hormone test system (A.1370) of the classification and grading management measures for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1370 Human Growth Hormone Testing System
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 10, 2024
- Expiry Date
- Sep 10, 2029
About this record
Access comprehensive regulatory information for Beckman Coulter Human Growth Hormone Reagent Set (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 a0d2be1b70f652ea38007be6ce779045 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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