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"Ashocore" Feihir gasification rod - Taiwan Registration 059e9e2dc2606ff4b5fa8ae65647034d

Access comprehensive regulatory information for "Ashocore" Feihir gasification rod in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 059e9e2dc2606ff4b5fa8ae65647034d and manufactured by ArthroCare Corporation. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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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059e9e2dc2606ff4b5fa8ae65647034d
Registration Details
Taiwan FDA Registration: 059e9e2dc2606ff4b5fa8ae65647034d
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Device Details

"Ashocore" Feihir gasification rod
TW: โ€œ้˜ฟ็ขฉๆŸฏ็ˆพโ€้ฃ›ๅธŒ็ˆพๆฐฃๅŒ–ๆฃ’
Risk Class 2

Registration Details

059e9e2dc2606ff4b5fa8ae65647034d

DHA05603700108

Company Information

Costa Rica;;United States

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4400 Cutting and hemostasis electric knives and accessories thereof

import

Dates and Status

Dec 26, 2023

Dec 26, 2028