Reasan Automatic cold light immunoassay analyzer (unsterilized)
Taiwan·Risk Class 1·DiaSorin Italia SpA·Registered Oct 04, 2021 – Oct 31, 2025Expired- Analysis ID
- 8b7630ec35ce6c9fcd5952525e290389
- Customs Code
- DHA084a0000201
- Manufacturer
- DiaSorin Italia SpA
- Manufacturer Country
- Italy
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
- 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
- Registration Date
- Oct 04, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for Reasan Automatic 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 8b7630ec35ce6c9fcd5952525e290389 and manufactured by DiaSorin Italia SpA. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DiaSorin Italia SpA, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.