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"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.

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f280271c09f51f40452169e6e2ac833e
Registration Details
Taiwan FDA Registration: f280271c09f51f40452169e6e2ac833e
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Device Details

"Americo" Clostridium difficile toxin A/B screening reagent (unsterilized)
TW: "ไบž็พŽๅˆฉๅฏ"ๅ›ฐ้›ฃๆขญ็‹€่Šฝ่ƒžๆกฟ่Œๆฏ’็ด A/B็ฏฉๆชข่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f280271c09f51f40452169e6e2ac833e

DHA09600248204

Company Information

China

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 ๅพฎ็”Ÿ็‰ฉ้‘‘ๅˆฅๅŠๆธฌๅฎšๅ™จๆ

Input;; Chinese goods

Dates and Status

Aug 27, 2015

Aug 27, 2020

Jun 22, 2022

Cancellation Information

Logged out

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