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“Cambridge” CRF Radiofrequency Ablation System - Taiwan Registration 4a35ac9f785e24356e24d0b1b0081d2c

Access comprehensive regulatory information for “Cambridge” CRF Radiofrequency Ablation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4a35ac9f785e24356e24d0b1b0081d2c 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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4a35ac9f785e24356e24d0b1b0081d2c
Registration Details
Taiwan FDA Registration: 4a35ac9f785e24356e24d0b1b0081d2c
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Device Details

“Cambridge” CRF Radiofrequency Ablation System
TW: “康橋”射頻消融手術電刀系統
Risk Class 2
MD

Registration Details

4a35ac9f785e24356e24d0b1b0081d2c

Ministry of Health Medical Device Import No. 035574

DHA05603557406

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

Jun 10, 2022

Jun 10, 2027