"ALIFAX" Microorganism differentiation and identification device (Non-Sterile) - Taiwan Registration aac6612425e6ab16efff8fb97640643b
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..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
aac6612425e6ab16efff8fb97640643b
Ministry of Health Medical Device Import No. 019802
DHA09401980208
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
C Immunology and microbiology devices
C2660 Microbial identification and assay equipment
Imported from abroad
Dates and Status
Nov 09, 2018
Nov 09, 2023