Taiwan FDA registration 067b04998b8561bbf5ff732730451fdc
"ALIFAX" Selective Supplements (Non-Sterile)
TW: "艾利福斯" 選擇性培養基添加劑 (未滅菌)
Taiwan·Risk Class 1·MD·Alifax S.r.l.·Registered Apr 18, 2019 – Apr 18, 2024ExpiredRegistration details
- Analysis ID
- 067b04998b8561bbf5ff732730451fdc
- License Form
- Ministry of Health Medical Device Import No. 020336
- Customs Code
- DHA09402033605
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 additives (C.2450) of the culture medium of the medical device management method.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- Additives to C2450 medium
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 18, 2019
- Expiry Date
- Apr 18, 2024
About this record
Access comprehensive regulatory information for "ALIFAX" Selective Supplements (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 067b04998b8561bbf5ff732730451fdc and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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