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“ENDO-FLEX” PTFE Biliary Stent - Taiwan Registration fd36d62d8719089c69893eb3b68f48f2

Access comprehensive regulatory information for “ENDO-FLEX” PTFE 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 fd36d62d8719089c69893eb3b68f48f2 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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fd36d62d8719089c69893eb3b68f48f2
Registration Details
Taiwan FDA Registration: fd36d62d8719089c69893eb3b68f48f2
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Device Details

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

Registration Details

fd36d62d8719089c69893eb3b68f48f2

Ministry of Health Medical Device Import No. 026996

DHA05602699605

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

Feb 16, 2015

Feb 16, 2025