"Americo" Clostridium difficile toxin A/B screening reagent (unsterilized) - Taiwan Registration f280271c09f51f40452169e6e2ac833e
Access comprehensive regulatory information for "Americo" Clostridium difficile toxin A/B screening reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f280271c09f51f40452169e6e2ac833e and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS 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
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
C.2660 ๅพฎ็็ฉ้ๅฅๅๆธฌๅฎๅจๆ
Input;; Chinese goods
Dates and Status
Aug 27, 2015
Aug 27, 2020
Jun 22, 2022
Cancellation Information
Logged out
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