Taiwan FDA registration ded646a0377ba4f76d191b80f30e8730
Vitex ECiQ Immunodiagnostic Analyzer (Unsterilized)
TW: 〝維特司〞ECiQ 免疫診斷分析儀 (未滅菌)
Taiwan·Risk Class 1·ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Sep 29, 2005 – Sep 29, 2025CancelledRegistration details
- Analysis ID
- ded646a0377ba4f76d191b80f30e8730
- Customs Code
- DHA04400065503
Company information
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS, INC
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
Product details
- Intended Use
- Clinical serum immunization program test analysis.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2560 Fluorometer for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Sep 29, 2005
- Expiry Date
- Sep 29, 2025
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for Vitex ECiQ Immunodiagnostic 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 ded646a0377ba4f76d191b80f30e8730 and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..
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