"Elifoss" Automated Media Kit (Unsterilized) - Taiwan Registration 8a28c3df74689fe94a743da99342045d
Access comprehensive regulatory information for "Elifoss" Automated Media Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8a28c3df74689fe94a743da99342045d 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
Product Details
It is limited to the first level of identification scope of the microbial growth monitor (C.2560) of the management measures for the classification and grading of medical devices.
C Immunology and microbiology
C.2560 Microbial growth monitors
Input;; QMS/QSD
Dates and Status
Mar 07, 2019
Mar 07, 2024