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Ruida Rapid Clostridium difficile toxin A/B antigen screening reagent (unsterilized) - Taiwan Registration 2a4bffd93d2fd9a51ac87ccd8ff2abf9

Access comprehensive regulatory information for Ruida Rapid Clostridium difficile toxin A/B antigen 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 2a4bffd93d2fd9a51ac87ccd8ff2abf9 and manufactured by R-BIOPHARM AG. The authorized representative in Taiwan is METEK LAB INC..

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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2a4bffd93d2fd9a51ac87ccd8ff2abf9
Registration Details
Taiwan FDA Registration: 2a4bffd93d2fd9a51ac87ccd8ff2abf9
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Device Details

Ruida Rapid Clostridium difficile toxin A/B antigen screening reagent (unsterilized)
TW: ็‘ž้”ๅฟซ้€Ÿ ๅ›ฐ้›ฃๆขญ็‹€่Šฝ่ƒžๆกฟ่Œๆฏ’็ด A/BๆŠ—ๅŽŸ็ฏฉๆชข่ฉฆๅŠ‘๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1

Registration Details

2a4bffd93d2fd9a51ac87ccd8ff2abf9

DHA04400922500

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Microbial Identification and Determination Equipment (C.2660)".

C Immunology and microbiology

C.2660 ๅพฎ็”Ÿ็‰ฉ้‘‘ๅˆฅๅŠๆธฌๅฎšๅ™จๆ

import

Dates and Status

Sep 21, 2010

Sep 21, 2025