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"Sterry" miniature biosensory forceps - Taiwan Registration 55d3e210524a130cd9ddd31c7714736f

Access comprehensive regulatory information for "Sterry" miniature biosensory forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55d3e210524a130cd9ddd31c7714736f and manufactured by STERIS CORPORATION;; UNITED STATES ENDOSCOPY GROUP, INC.. The authorized representative in Taiwan is Sterry Taiwan Corporation.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STERIS CORPORATION;; UNITED STATES ENDOSCOPY GROUP, INC., 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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55d3e210524a130cd9ddd31c7714736f
Registration Details
Taiwan FDA Registration: 55d3e210524a130cd9ddd31c7714736f
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Device Details

"Sterry" miniature biosensory forceps
TW: "ๅฒๆณฐ็‘ž" ๅพฎๅž‹็”Ÿๆชข้‰—
Risk Class 2

Registration Details

55d3e210524a130cd9ddd31c7714736f

DHA05603443401

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.1075 ่…ธ่ƒƒ็ง‘-ๆณŒๅฐฟ็ง‘็”Ÿๆชขๅ™จๆขฐ

import

Dates and Status

Apr 16, 2021

Apr 16, 2026

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