Taiwan FDA registration c9f0ac7bdb28d7eb0ed5691f53e40bab
Vetex Biochemical Products No. 6 Correction Solution
TW: 維特司生化產品6號校正液
Registration details
- Analysis ID
- c9f0ac7bdb28d7eb0ed5691f53e40bab
- Customs Code
- DHA00601208602
Company information
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS, INC
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
Product details
- Intended Use
- Vetex 6 Correction Solution is used to correct the quantitative measurement of Vetex biochemical system isomeric per chole lipid and muscle base per isomeric component. The following blank change performance (new applicable models) is: For in vitro diagnostic use only. This product is used to correct the quantitative measurement of bilifibrosterase and myosylase isomerase in the Vitex biochemical system. This product is required for use with the Vitex 350/5,1 FS/4600/XT3400 chemical analyzer and the Vitex 5600/XT7600 biochemical immunoassay analyzer. The following blanks
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Aug 18, 2005
- Expiry Date
- Aug 18, 2025
About this record
Access comprehensive regulatory information for Vetex Biochemical Products No. 6 Correction Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c9f0ac7bdb28d7eb0ed5691f53e40bab and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..
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