Taiwan FDA registration aac6612425e6ab16efff8fb97640643b

"ALIFAX" Microorganism differentiation and identification device (Non-Sterile)

TW: "艾利福斯" 微生物鑑別及測定器材 (未滅菌)

Taiwan·Risk Class 1·MD·Alifax S.r.l.·Registered Nov 09, 2018 – Nov 09, 2023Expired

Registration details

Analysis ID: aac6612425e6ab16efff8fb97640643b
License Form: Ministry of Health Medical Device Import No. 019802
Customs Code: DHA09401980208

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 Identification and Measurement Equipment (C.2660)".
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C2660 Microbial identification and assay equipment
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" Microorganism differentiation and identification 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 aac6612425e6ab16efff8fb97640643b and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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