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“DAIWHA” Meditom Ultra-Electro Surgical unit - Taiwan Registration 66f30c72980d1d59100a33a116d658f0

Access comprehensive regulatory information for “DAIWHA” Meditom Ultra-Electro Surgical unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 66f30c72980d1d59100a33a116d658f0 and manufactured by Daiwha Corp. Ltd.. The authorized representative in Taiwan is SOAR INSTRUMENT-TECH. 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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66f30c72980d1d59100a33a116d658f0
Registration Details
Taiwan FDA Registration: 66f30c72980d1d59100a33a116d658f0
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Device Details

“DAIWHA” Meditom Ultra-Electro Surgical unit
TW: “大華”麥德塔外科手術系統
Risk Class 2
MD

Registration Details

66f30c72980d1d59100a33a116d658f0

Ministry of Health Medical Device Import No. 034123

DHA05603412307

Company Information

Korea, Republic of

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

Dec 13, 2020

Dec 13, 2025