Taiwan FDA registration 5854e58f699854b52cf89ef3e80c50b3
"ALIFAX" Microbiological specimen collection and transport device (Non-Sterile)
TW: "艾利福斯" 微生物樣本收集及輸送器材 (未滅菌)
Taiwan·Risk Class 1·MD·Alifax S.r.l.·Registered Oct 26, 2018 – Oct 26, 2023ExpiredRegistration details
- Analysis ID
- 5854e58f699854b52cf89ef3e80c50b3
- License Form
- Ministry of Health Medical Device Import No. 019730
- Customs Code
- DHA09401973009
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 Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2900 Microbial sample collection and delivery device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 26, 2018
- Expiry Date
- Oct 26, 2023
About this record
Access comprehensive regulatory information for "ALIFAX" Microbiological specimen collection and transport device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5854e58f699854b52cf89ef3e80c50b3 and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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