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"Sterry" single-use slicing valve - Taiwan Registration 303123526b7516ce1b15a3b6c078eacf

Access comprehensive regulatory information for "Sterry" single-use slicing valve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 303123526b7516ce1b15a3b6c078eacf and manufactured by STERIS Corporation;; UNITED STATES ENDOSCOPY GROUP, INC.. The authorized representative in Taiwan is MEDTRUST INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including UNITED STATES ENDOSCOPY GROUP, INC.;; STERIS Corporation, and 1 recent registrations in the same category. 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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303123526b7516ce1b15a3b6c078eacf
Registration Details
Taiwan FDA Registration: 303123526b7516ce1b15a3b6c078eacf
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Device Details

"Sterry" single-use slicing valve
TW: โ€œๆ€ๆณฐ็‘žโ€ๅ–ฎๆฌกไฝฟ็”จๅˆ‡็‰‡้–ฅ้–€
Risk Class 2

Registration Details

303123526b7516ce1b15a3b6c078eacf

DHA05603738806

Company Information

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Sep 03, 2024

Sep 03, 2029

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