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“ENDO-FLEX” Guide Wires - Taiwan Registration 9b3d377aa5c236fe177486157770173d

Access comprehensive regulatory information for “ENDO-FLEX” Guide Wires in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9b3d377aa5c236fe177486157770173d 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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9b3d377aa5c236fe177486157770173d
Registration Details
Taiwan FDA Registration: 9b3d377aa5c236fe177486157770173d
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Device Details

“ENDO-FLEX” Guide Wires
TW: “福萊克斯”導引線
Risk Class 2
MD

Registration Details

9b3d377aa5c236fe177486157770173d

Ministry of Health Medical Device Import No. 028570

DHA05602857007

Company Information

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

May 10, 2016

May 10, 2026