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"Covidien" Iriss RF ablation accessories - Taiwan Registration 196589b3a6ffd4cc4536cf29bc8c4628

Access comprehensive regulatory information for "Covidien" Iriss RF ablation accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 196589b3a6ffd4cc4536cf29bc8c4628 and manufactured by Covidien llc;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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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196589b3a6ffd4cc4536cf29bc8c4628
Registration Details
Taiwan FDA Registration: 196589b3a6ffd4cc4536cf29bc8c4628
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Device Details

"Covidien" Iriss RF ablation accessories
TW: โ€œๆŸฏๆƒ โ€ๆ˜“็‘žๅธๅฐ„้ ปๆถˆ่ž้…ไปถ
Risk Class 2

Registration Details

196589b3a6ffd4cc4536cf29bc8c4628

DHA05603645901

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4400 Cutting and hemostasis electric knives and accessories thereof

import

Dates and Status

Mar 31, 2023

Mar 31, 2028