Taiwan FDA registration 7e723d515948039aca310ec6a8aa251e
Vitex Biochemical Products Direct HDL Cholesterol Test Tablets
TW: 維特司生化產品直接高密度脂蛋白膽固醇試藥片
Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Mar 08, 2006 – Mar 08, 2016CancelledRegistration details
- Analysis ID
- 7e723d515948039aca310ec6a8aa251e
- Customs Code
- DHA00601611401
Company information
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
Product details
- Intended Use
- It is used to quantitatively determine the concentration of high-density lipoprotein cholesterol in serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1475 Lipoprotein Testing System
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2006
- Expiry Date
- Mar 08, 2016
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Vitex Biochemical Products Direct HDL Cholesterol Test Tablets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e723d515948039aca310ec6a8aa251e and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..
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