Vitex Biochemical Products Drug Abuse Special Pharmaceutical Control Solution (Unsterilized)
Taiwan·Risk Class 1·ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered May 18, 2007 – May 18, 2017Cancelled- Analysis ID
- 1077becdb12e0434a81e58cec77bda7f
- Customs Code
- DHA04400586500
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
- Registration Date
- May 18, 2007
- Expiry Date
- May 18, 2017
- Cancellation Date
- Jan 09, 2017
- Status
- Logged out
- Reason
- 自行鍵入
Access comprehensive regulatory information for Vitex Biochemical Products Drug Abuse Special Pharmaceutical Control Solution (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1077becdb12e0434a81e58cec77bda7f and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.