Taiwan FDA registration f94371af3ea1b533960ec8950340b4ef
Vitex Biochemical Products Liquid Quality Confirmation Liquid I and II
TW: 維特司生化產品液狀品質確認液I 和 II
Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Sep 20, 2005 – Sep 20, 2025ExpiredRegistration details
- Analysis ID
- f94371af3ea1b533960ec8950340b4ef
- Customs Code
- DHA00601244603
Company information
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS, INC
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
Product details
- Intended Use
- Limited to in vitro diagnostic use. This product is a known concentration of quality control solution, which is used to monitor the performance of the liquid on the Vitex biochemical system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Sep 20, 2005
- Expiry Date
- Sep 20, 2025
About this record
Access comprehensive regulatory information for Vitex Biochemical Products Liquid Quality Confirmation Liquid I and II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f94371af3ea1b533960ec8950340b4ef and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..
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