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"R-Biopharm" RIDA QUICK Clostridium difficile Toxin A/B Control (Non-sterile) - Taiwan Registration 0396b8a64ad8b056b5ad576f87e08e1e

Access comprehensive regulatory information for "R-Biopharm" RIDA QUICK Clostridium difficile Toxin A/B Control (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 0396b8a64ad8b056b5ad576f87e08e1e 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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0396b8a64ad8b056b5ad576f87e08e1e
Registration Details
Taiwan FDA Registration: 0396b8a64ad8b056b5ad576f87e08e1e
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Device Details

"R-Biopharm" RIDA QUICK Clostridium difficile Toxin A/B Control (Non-sterile)
TW: "ๅšๆ–น" ๅ›ฐ้›ฃๆขญ็‹€ๆกฟ่Œๆฏ’็ด A/Bๅ“็ฎกๆถฒ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

0396b8a64ad8b056b5ad576f87e08e1e

Ministry of Health Medical Device Import No. 015836

DHA09401583605

Company Information

Germany

Product Details

Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Nov 10, 2015

Nov 10, 2025