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“HANIL-TM” Extracorporeal Shock Wave Therapy - Taiwan Registration bee509d3db5f337e10c36cdec9f7c9f1

Access comprehensive regulatory information for “HANIL-TM” Extracorporeal Shock Wave Therapy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bee509d3db5f337e10c36cdec9f7c9f1 and manufactured by HANIL-TM CO., LTD.. The authorized representative in Taiwan is HUA YI INTERNATIONAL 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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bee509d3db5f337e10c36cdec9f7c9f1
Registration Details
Taiwan FDA Registration: bee509d3db5f337e10c36cdec9f7c9f1
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Device Details

“HANIL-TM” Extracorporeal Shock Wave Therapy
TW: “韓尼爾堤”體外震波治療儀
Risk Class 3
MD

Registration Details

bee509d3db5f337e10c36cdec9f7c9f1

Ministry of Health Medical Device Import No. 028723

DHA05602872306

Company Information

Korea, Republic of

Product Details

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

N Orthopedic devices

N0001 Extracorporeal shock wave system for orthopedics

Imported from abroad

Dates and Status

Aug 09, 2016

Aug 09, 2026