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“Arthrex” Synergy RF System - Taiwan Registration 46ddb759d8a55f8cca77e336ceff4b62

Access comprehensive regulatory information for “Arthrex” Synergy RF System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46ddb759d8a55f8cca77e336ceff4b62 and manufactured by Arthrex, Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Arthrex Inc., and 1 recent registrations in the same category. 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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46ddb759d8a55f8cca77e336ceff4b62
Registration Details
Taiwan FDA Registration: 46ddb759d8a55f8cca77e336ceff4b62
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Device Details

“Arthrex” Synergy RF System
TW: “艾思瑞斯”電燒系統
Risk Class 2
MD

Registration Details

46ddb759d8a55f8cca77e336ceff4b62

Ministry of Health Medical Device Import No. 034118

DHA05603411801

Company Information

United States

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 29, 2020

Nov 29, 2025

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