Taiwan FDA registration 76bb6cda7460350520fde86620966b33
Reasan Desktop Automatic Chemical Cold Light Immunoassay Analyzer (Unsterilized)
TW: 禮亞尚 桌上型全自動化學冷光免疫分析儀(未滅菌)
Taiwan·Risk Class 1·DiaSorin Italia SpA·Registered Oct 04, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 76bb6cda7460350520fde86620966b33
- Customs Code
- DHA084a0000102
Company information
- Manufacturer
- DiaSorin Italia SpA
- Manufacturer Country
- Italy
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Dates and status
- Registration Date
- Oct 04, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Reasan Desktop Automatic Chemical Cold Light Immunoassay 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 76bb6cda7460350520fde86620966b33 and manufactured by DiaSorin Italia SpA. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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