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"Covidien" scouring tonsillectomy device - Taiwan Registration de1b309d62d99b86d6cdb8d940ad78cc

Access comprehensive regulatory information for "Covidien" scouring tonsillectomy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de1b309d62d99b86d6cdb8d940ad78cc and manufactured by COVIDIEN LLC;; COVID. 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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de1b309d62d99b86d6cdb8d940ad78cc
Registration Details
Taiwan FDA Registration: de1b309d62d99b86d6cdb8d940ad78cc
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Device Details

"Covidien" scouring tonsillectomy device
TW: โ€œๆŸฏๆƒ โ€็™พๆฝ”ๆ‰ๆกƒ่…บๅˆ‡้™ค่ฃ็ฝฎ
Risk Class 2

Registration Details

de1b309d62d99b86d6cdb8d940ad78cc

DHA05603610107

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

Nov 22, 2022

Nov 22, 2027