Taiwan FDA registration e08d98230893d01b6fb0ba9e46124e39
Diascot Immunoassay System (Unsterilized)
TW: 〝迪雅仕〞可錄思 免疫試驗系統 (未滅菌)
Taiwan·Risk Class 1·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered Mar 27, 2013 – Mar 27, 2023ExpiredRegistration details
- Analysis ID
- e08d98230893d01b6fb0ba9e46124e39
- Customs Code
- DHA04401284409
Company information
- Manufacturer
- DIESSE DIAGNOSTICA SENESE S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Human Whole Plasma or Serum Immunoassay System (C.5700)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5700 Human whole plasma or serum immunoassay system
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 27, 2013
- Expiry Date
- Mar 27, 2023
About this record
Access comprehensive regulatory information for Diascot Immunoassay System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e08d98230893d01b6fb0ba9e46124e39 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices