Taiwan FDA registration 059e9e2dc2606ff4b5fa8ae65647034d

"Ashocore" Feihir gasification rod

TW: “阿碩柯爾”飛希爾氣化棒

Taiwan·Risk Class 2·ArthroCare Corporation·Registered Dec 26, 2023 – Dec 26, 2028Active

Registration details

Analysis ID: 059e9e2dc2606ff4b5fa8ae65647034d
Customs Code: DHA05603700108

Company information

Manufacturer: ArthroCare Corporation
Manufacturer Country: Costa Rica;;United States
Authorized Representative: SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4400 Cutting and hemostasis electric knives and accessories thereof
Import Information: import

Dates and status

Registration Date: Dec 26, 2023
Expiry Date: Dec 26, 2028

About this record

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.