Taiwan FDA registration 17b545e581d052a0fc0e738485b5351b
Vitex immunodiagnostic high-value sample diluent B reagent set
TW: 維特司免疫診斷高值檢體稀釋液B 試劑組
Taiwan·Risk Class 1·ORTHO-CLINICAL DIAGNOSTICS·Registered Oct 18, 2010 – Oct 18, 2015CancelledRegistration details
- Analysis ID
- 17b545e581d052a0fc0e738485b5351b
- Customs Code
- DHA04400938200
Company information
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS
- Manufacturer Country
- United Kingdom
- Authorized Representative
- DKSH TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4010 Reaction Reagents for General Purposes
- Import Information
- import
Dates and status
- Registration Date
- Oct 18, 2010
- Expiry Date
- Oct 18, 2015
- 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 immunodiagnostic high-value sample diluent B reagent set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 17b545e581d052a0fc0e738485b5351b and manufactured by ORTHO-CLINICAL DIAGNOSTICS. The authorized representative in Taiwan is DKSH TAIWAN LTD..
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