Pure Global

“ArthroCare” Coblator II System - Taiwan Registration dcbae27360aeefb7ee4ef5484cfe0bf1

Access comprehensive regulatory information for “ArthroCare” Coblator II System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dcbae27360aeefb7ee4ef5484cfe0bf1 and manufactured by SMITH & NEPHEW, INC. ENDOSCOPY DIVISION. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
dcbae27360aeefb7ee4ef5484cfe0bf1
Registration Details
Taiwan FDA Registration: dcbae27360aeefb7ee4ef5484cfe0bf1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“ArthroCare” Coblator II System
TW: “阿碩柯爾”電刀系統
Risk Class 2
MD

Registration Details

dcbae27360aeefb7ee4ef5484cfe0bf1

Ministry of Health Medical Device Import No. 030396

DHA05603039609

Company Information

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

Nov 14, 2017

Nov 14, 2027