"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized)
Taiwan·Risk Class 1·DiaSorin Italia SpA·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 6cdd22d4af6bd15054a874b88b498343
- Customs Code
- DHA08402012407
- Manufacturer
- DiaSorin Italia SpA
- Manufacturer Country
- Italy
- Authorized Representative
- MEDRICH INSTRUMENT 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
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Oct 01, 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 6cdd22d4af6bd15054a874b88b498343 and manufactured by DiaSorin Italia SpA. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DIASORIN S.P.A., DIASORIN DEUTSCHLAND GMBH, and 2 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.