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“DERMACARE” EDISC Bipolar Electrode - Taiwan Registration 38d9f0ac1af3aed77b399cc8cedb2380

Access comprehensive regulatory information for “DERMACARE” EDISC Bipolar Electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38d9f0ac1af3aed77b399cc8cedb2380 and manufactured by DERMACARE BIOMED INC.. The authorized representative in Taiwan is DERMACARE BIOMED INC..

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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38d9f0ac1af3aed77b399cc8cedb2380
Registration Details
Taiwan FDA Registration: 38d9f0ac1af3aed77b399cc8cedb2380
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Device Details

“DERMACARE” EDISC Bipolar Electrode
TW: “德瑪凱”易速凝雙極電燒器
Risk Class 2
MD

Registration Details

38d9f0ac1af3aed77b399cc8cedb2380

Ministry of Health Medical Device Manufacturing No. 007054

Company Information

Taiwan, Province of China

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

Produced in Taiwan, China

Dates and Status

Jan 13, 2021

Jun 16, 2025