Taiwan FDA registration 882d4e1289b80c345fc16bf537fe9f4c
"ALIFAX" Enriched culture medium (Non-Sterile)
TW: "艾利福斯" 強化培養基 (未滅菌)
Taiwan·Risk Class 1·MD·Alifax S.r.l.·Registered Nov 09, 2018 – Nov 09, 2023ExpiredRegistration details
- Analysis ID
- 882d4e1289b80c345fc16bf537fe9f4c
- License Form
- Ministry of Health Medical Device Import No. 019804
- Customs Code
- DHA09401980402
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 range of the Measures for the Administration of Medical Devices "Intensive Medium (C.2330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2330 fortified medium
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 09, 2018
- Expiry Date
- Nov 09, 2023
About this record
Access comprehensive regulatory information for "ALIFAX" Enriched culture medium (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 882d4e1289b80c345fc16bf537fe9f4c and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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