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“R-BIOPHARM” RIDAGENE Clostridium difficile (Non-Sterile) - Taiwan Registration 8dfd71c2d51cf3e2c528fe03fc4ac2fa

Access comprehensive regulatory information for “R-BIOPHARM” RIDAGENE Clostridium difficile (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 8dfd71c2d51cf3e2c528fe03fc4ac2fa 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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8dfd71c2d51cf3e2c528fe03fc4ac2fa
Registration Details
Taiwan FDA Registration: 8dfd71c2d51cf3e2c528fe03fc4ac2fa
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Device Details

“R-BIOPHARM” RIDAGENE Clostridium difficile (Non-Sterile)
TW: “博方”困難梭狀桿菌檢測試劑 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

8dfd71c2d51cf3e2c528fe03fc4ac2fa

Ministry of Health Medical Device Import No. 014698

DHA09401469801

Company Information

Germany

Product Details

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Nov 24, 2014

Nov 24, 2019

May 06, 2019

Cancellation Information

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