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"R-BIOPHARM" Clostridium difficile GDH (Non-Sterile) - Taiwan Registration 196b8b3457d1f342d04cbef811167748

Access comprehensive regulatory information for "R-BIOPHARM" Clostridium difficile GDH (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 196b8b3457d1f342d04cbef811167748 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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196b8b3457d1f342d04cbef811167748
Registration Details
Taiwan FDA Registration: 196b8b3457d1f342d04cbef811167748
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Device Details

"R-BIOPHARM" Clostridium difficile GDH (Non-Sterile)
TW: "ๅšๆ–น"ๅ›ฐ้›ฃๆขญ็‹€ๆกฟ่ŒๆŠ—ๅŽŸๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

196b8b3457d1f342d04cbef811167748

Ministry of Health Medical Device Import No. 013883

DHA09401388304

Company Information

Germany

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 devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Feb 25, 2014

Feb 25, 2024