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B. Braun Serpia Hydrophilic Guiding Catheter - Taiwan Registration 50daf27d9e583df833fe457185a719df

Access comprehensive regulatory information for B. Braun Serpia Hydrophilic Guiding Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50daf27d9e583df833fe457185a719df and manufactured by PENDRACARE INTERNATIONAL B.V.. The authorized representative in Taiwan is B. BRAUN TAIWAN 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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50daf27d9e583df833fe457185a719df
Registration Details
Taiwan FDA Registration: 50daf27d9e583df833fe457185a719df
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Device Details

B. Braun Serpia Hydrophilic Guiding Catheter
TW: ๆŸๆœ—ๅฐŽๅผ•ๅฐŽ็ฎก
Risk Class 2
MD

Registration Details

50daf27d9e583df833fe457185a719df

Ministry of Health Medical Device Import No. 025668

DHA05602566809

Company Information

Netherlands

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Dec 17, 2013

Dec 17, 2023