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“Argon” Vessel Dilators - Taiwan Registration 34526e6059a0c78fa173a7fe19f056e8

Access comprehensive regulatory information for “Argon” Vessel Dilators in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 34526e6059a0c78fa173a7fe19f056e8 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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34526e6059a0c78fa173a7fe19f056e8
Registration Details
Taiwan FDA Registration: 34526e6059a0c78fa173a7fe19f056e8
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Device Details

“Argon” Vessel Dilators
TW: “亞康恩”血管擴張器
Risk Class 2
MD

Registration Details

34526e6059a0c78fa173a7fe19f056e8

Ministry of Health Medical Device Import No. 032079

DHA05603207907

Company Information

United States

Product Details

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

E Cardiovascular devices

E1310 Vasodilator for percutaneous catheters

Imported from abroad

Dates and Status

Jan 18, 2019

Jan 18, 2029