"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.
Free Database
Powered by Pure Global AI
89,000+ Devices
292a1201f95bdc4853032bdfe834409a
Registration Details
Taiwan FDA Registration: 292a1201f95bdc4853032bdfe834409a
Device Details
"Aegis Medical" single-use biopsy forceps
TW: โๅฎๆฐๆ้ซๅญธโไธๆฌกๆงไฝฟ็จๆดป็ต็นๅๆจฃ้
Risk Class 2

