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“Cambridge” CRF Electrode System - Taiwan Registration e76280af0008184b0c8af82551ebc18e

Access comprehensive regulatory information for “Cambridge” CRF Electrode System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e76280af0008184b0c8af82551ebc18e and manufactured by Cambridge Interventional LLC. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..

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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e76280af0008184b0c8af82551ebc18e
Registration Details
Taiwan FDA Registration: e76280af0008184b0c8af82551ebc18e
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Device Details

“Cambridge” CRF Electrode System
TW: “康橋”射頻手術電極系統
Risk Class 2
MD

Registration Details

e76280af0008184b0c8af82551ebc18e

Ministry of Health Medical Device Import No. 035468

DHA05603546807

Company Information

United States

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

May 10, 2022

May 10, 2027