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“Syneron” eTwo System - Taiwan Registration 6a8b39ed1b1df8be2ac14e182ca4f9c6

Access comprehensive regulatory information for “Syneron” eTwo System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6a8b39ed1b1df8be2ac14e182ca4f9c6 and manufactured by SYNERON MEDICAL LTD.. The authorized representative in Taiwan is YUNGLIN BIOTECHNOLOGY CO., LTD..

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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6a8b39ed1b1df8be2ac14e182ca4f9c6
Registration Details
Taiwan FDA Registration: 6a8b39ed1b1df8be2ac14e182ca4f9c6
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Device Details

“Syneron” eTwo System
TW: “新那隆”伊特電波除皺系統
Risk Class 2
MD

Registration Details

6a8b39ed1b1df8be2ac14e182ca4f9c6

Ministry of Health Medical Device Import No. 025959

DHA05602595907

Company Information

Israel

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 05, 2015

May 23, 2024