Taiwan FDA registration 68e5b0f0d4cac3100def9a891a985acb
VITROS ECiQ Immunodiagnostics System (Non-Sterile)
TW: 〝維特司〞ECiQ 免疫診斷分析儀 (未滅菌)
Taiwan·Risk Class 1·MD·ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 68e5b0f0d4cac3100def9a891a985acb
- License Form
- Ministry of Health Medical Device Import Registration No. 000655
- Customs Code
- DHA08400065500
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)
- A2560 fluorometer for clinical use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for VITROS ECiQ Immunodiagnostics System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 68e5b0f0d4cac3100def9a891a985acb and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC. The authorized representative in Taiwan is DKSH TAIWAN LTD..
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