Taiwan FDA registration 05f2e8e5b28532137e320df0fb3a5129
AutoDELFIA Automated Immunoassay System（Non-Sterile）
TW: 歐圖岱奧菲自動免疫分析系統（未滅菌）
Taiwan·Risk Class 1·MD·WALLAC OY·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 05f2e8e5b28532137e320df0fb3a5129
- License Form
- Ministry of Health Medical Device Import Registration No. 000781
- Customs Code
- DHA08400078105
Company information
- Manufacturer
- WALLAC OY
- Manufacturer Country
- Finland
- Authorized Representative
- FENG CHI BIOTECH CORP.
Product details
- Intended Use
- Fully automatic jet lag fluorometer.
- 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 AutoDELFIA Automated Immunoassay 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 05f2e8e5b28532137e320df0fb3a5129 and manufactured by WALLAC OY. The authorized representative in Taiwan is FENG CHI BIOTECH CORP..
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