Taiwan FDA registration 69d25b99b7d1d2b4f191ca3a1a3a8b6d
Vitex immunodiagnostic cleansing solution
TW: 維特司免疫診斷清洗液
Taiwan·Risk Class 1·ORTHO-CLINICAL DIAGNOSTICS·Registered Oct 18, 2010 – Oct 18, 2015CancelledRegistration details
- Analysis ID
- 69d25b99b7d1d2b4f191ca3a1a3a8b6d
- Customs Code
- DHA04400938101
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 cleansing solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 69d25b99b7d1d2b4f191ca3a1a3a8b6d and manufactured by ORTHO-CLINICAL DIAGNOSTICS. The authorized representative in Taiwan is DKSH TAIWAN LTD..
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