"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized)
Taiwan·Risk Class 1·DIASORIN DEUTSCHLAND GMBH·Registered Oct 01, 2021 – Oct 31, 2022Cancelled- Analysis ID
- 2025307f700917dc03228d1721f749cb
- Customs Code
- DHA08401757300
- Manufacturer
- DIASORIN DEUTSCHLAND GMBH
- Manufacturer Country
- Germany
- 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
- Input;; QMS/QSD
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
- Cancellation Date
- Feb 01, 2023
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 2025307f700917dc03228d1721f749cb and manufactured by DIASORIN DEUTSCHLAND GMBH. 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 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.