Taiwan FDA registration 59b8a20f65204e7d9a24adf884f64aa8
"Elifoss" Microbial Identification and Determination Equipment (Unsterilized)
TW: "艾利福斯" 微生物鑑別與測定器材 (未滅菌)
Taiwan·Risk Class 1·Alifax S.r.l.·Registered Sep 16, 2020 – Sep 16, 2025ExpiredRegistration details
- Analysis ID
- 59b8a20f65204e7d9a24adf884f64aa8
- Customs Code
- DHA09402196502
Company information
- Manufacturer
- Alifax S.r.l.
- Manufacturer Country
- Italy
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Microbial Identification and Determination Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2660 微生物鑑別及測定器材
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 16, 2020
- Expiry Date
- Sep 16, 2025
About this record
Access comprehensive regulatory information for "Elifoss" Microbial Identification and Determination Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 59b8a20f65204e7d9a24adf884f64aa8 and manufactured by Alifax S.r.l.. 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