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“DAIWHA” Meditom Electrosurgical unit - Taiwan Registration f7c65f382616000c384fc10ca7aeea28

Access comprehensive regulatory information for “DAIWHA” Meditom Electrosurgical unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f7c65f382616000c384fc10ca7aeea28 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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f7c65f382616000c384fc10ca7aeea28
Registration Details
Taiwan FDA Registration: f7c65f382616000c384fc10ca7aeea28
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Device Details

“DAIWHA” Meditom Electrosurgical unit
TW: “大華”麥德塔電刀系統
Risk Class 2
MD

Registration Details

f7c65f382616000c384fc10ca7aeea28

Ministry of Health Medical Device Import No. 036297

DHA05603629701

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Feb 03, 2023

Feb 03, 2028