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“ENDO-FLEX” Biliary Stent - Taiwan Registration faf82b5738512e788ef277d2dd9376e2

Access comprehensive regulatory information for “ENDO-FLEX” Biliary Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number faf82b5738512e788ef277d2dd9376e2 and manufactured by ENDO-FLEX GmbH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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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faf82b5738512e788ef277d2dd9376e2
Registration Details
Taiwan FDA Registration: faf82b5738512e788ef277d2dd9376e2
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Device Details

“ENDO-FLEX” Biliary Stent
TW: “福萊克斯”膽道引流管
Risk Class 2
MD

Registration Details

faf82b5738512e788ef277d2dd9376e2

Ministry of Health Medical Device Import No. 027489

DHA05602748906

Company Information

Product Details

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

H Gastroenterology-urology devices

H5010 Bile ductal catheters and their accessories

Imported from abroad

Dates and Status

Jul 03, 2015

Jul 03, 2025