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“Argon” Guidewire Introducer Needles - Taiwan Registration a0b9a2cb1f14ca89b774408e36a4910a

Access comprehensive regulatory information for “Argon” Guidewire Introducer Needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0b9a2cb1f14ca89b774408e36a4910a and manufactured by ARGON MEDICAL DEVICES INC.. The authorized representative in Taiwan is CHINA SPRING TRADING 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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a0b9a2cb1f14ca89b774408e36a4910a
Registration Details
Taiwan FDA Registration: a0b9a2cb1f14ca89b774408e36a4910a
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Device Details

“Argon” Guidewire Introducer Needles
TW: “亞康恩”導引線導引針
Risk Class 2
MD

Registration Details

a0b9a2cb1f14ca89b774408e36a4910a

Ministry of Health Medical Device Import No. 028238

DHA05602823802

Company Information

United States

Product Details

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

E Cardiovascular devices

E1340 Catheter Guide

Imported from abroad

Dates and Status

Feb 19, 2016

Feb 19, 2026