Taiwan FDA registration 4b1e029cbae5a8b44c258975f19744ca
"ALIFAX" POSITIVE CONTROL KIT (Non-Sterile)
TW: "艾利福斯"陽性品管套組(未滅菌)
Taiwan·Risk Class 1·MD·Alifax S.r.l.·Registered Dec 03, 2018 – Dec 03, 2023ExpiredRegistration details
- Analysis ID
- 4b1e029cbae5a8b44c258975f19744ca
- License Form
- Ministry of Health Medical Device Import No. 019871
- Customs Code
- DHA09401987101
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 quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 03, 2018
- Expiry Date
- Dec 03, 2023
About this record
Access comprehensive regulatory information for "ALIFAX" POSITIVE CONTROL KIT (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 4b1e029cbae5a8b44c258975f19744ca and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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