"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized)
Taiwan·Risk Class 1·DIASORIN S.P.A.·Registered Feb 26, 2019 – Feb 26, 2024Cancelled- Analysis ID
- 07a261af4beea75477cc665ace963b32
- Customs Code
- DHA09402012403
- Manufacturer
- DIASORIN S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration 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
- Feb 26, 2019
- Expiry Date
- Feb 26, 2024
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 07a261af4beea75477cc665ace963b32 and manufactured by DIASORIN S.P.A.. 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 DEUTSCHLAND GMBH, DiaSorin Italia SpA, 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.