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"Aegis Medical" single-use biopsy forceps - Taiwan Registration 292a1201f95bdc4853032bdfe834409a

Access comprehensive regulatory information for "Aegis Medical" single-use biopsy forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 292a1201f95bdc4853032bdfe834409a and manufactured by Hangzhou AGS MedTech Co., Ltd.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., 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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292a1201f95bdc4853032bdfe834409a
Registration Details
Taiwan FDA Registration: 292a1201f95bdc4853032bdfe834409a
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Device Details

"Aegis Medical" single-use biopsy forceps
TW: โ€œๅฎ‰ๆฐๆ€้†ซๅญธโ€ไธ€ๆฌกๆ€งไฝฟ็”จๆดป็ต„็น”ๅ–ๆจฃ้‰—
Risk Class 2

Registration Details

292a1201f95bdc4853032bdfe834409a

DHA09200131908

Company Information

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

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

Input;; Chinese goods

Dates and Status

Apr 26, 2022

Apr 26, 2027