Taiwan FDA registration ffe34fd2b92d38edae32aad065b9d52a
"Vitex" 950 Chemical Analyzer (Unsterilized)
TW: "維特司" 950 化學分析儀(未滅菌)
Taiwan·Risk Class 1·ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Sep 28, 2005 – Sep 28, 2015CancelledRegistration details
- Analysis ID
- ffe34fd2b92d38edae32aad065b9d52a
- Customs Code
- DHA04400063204
Company information
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS, INC
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
Product details
- Intended Use
- Clinical biochemical project test analysis.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Import Information
- import
Dates and status
- Registration Date
- Sep 28, 2005
- Expiry Date
- Sep 28, 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" 950 Chemical Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ffe34fd2b92d38edae32aad065b9d52a and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..
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