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“Kirwan” Reusable Bipolar Forceps - Taiwan Registration 236a79b58426ad08e9ae425d460f05df

Access comprehensive regulatory information for “Kirwan” Reusable Bipolar Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 236a79b58426ad08e9ae425d460f05df and manufactured by KIRWAN SURGICAL PRODUCTS, LLC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

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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236a79b58426ad08e9ae425d460f05df
Registration Details
Taiwan FDA Registration: 236a79b58426ad08e9ae425d460f05df
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Device Details

“Kirwan” Reusable Bipolar Forceps
TW: “柯恩”可重複使用雙極電燒鑷子
Risk Class 2
MD

Registration Details

236a79b58426ad08e9ae425d460f05df

Ministry of Health Medical Device Import No. 030997

DHA05603099709

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

Mar 23, 2018

Mar 23, 2028