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“RF” ablation system and Accessories - Taiwan Registration 63435cc0d17b4eb72c80cb2a9980db4e

Access comprehensive regulatory information for “RF” ablation system and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 63435cc0d17b4eb72c80cb2a9980db4e and manufactured by RF MEDICAL CO., LTD. The authorized representative in Taiwan is GOLEAD BIOPHARM INC..

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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63435cc0d17b4eb72c80cb2a9980db4e
Registration Details
Taiwan FDA Registration: 63435cc0d17b4eb72c80cb2a9980db4e
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Device Details

“RF” ablation system and Accessories
TW: “艾爾發”電子燒灼機及其附件
Risk Class 2
MD

Registration Details

63435cc0d17b4eb72c80cb2a9980db4e

Ministry of Health Medical Device Import No. 029602

DHA05602960202

Company Information

Korea, Republic of

Product Details

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

I General and plastic surgical devices

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Mar 15, 2017

Mar 15, 2022