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“Volcano” CORE Mobile Precision Guided Therapy System - Taiwan Registration a3aade4f9c62c359e91aab7daa45a68c

Access comprehensive regulatory information for “Volcano” CORE Mobile Precision Guided Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3aade4f9c62c359e91aab7daa45a68c and manufactured by Volcano Corporation. The authorized representative in Taiwan is LORION ENTERPRISES INC..

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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a3aade4f9c62c359e91aab7daa45a68c
Registration Details
Taiwan FDA Registration: a3aade4f9c62c359e91aab7daa45a68c
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Device Details

“Volcano” CORE Mobile Precision Guided Therapy System
TW: “火山” 彩色血管內超音波及血流量分析系統
Risk Class 2
MD

Registration Details

a3aade4f9c62c359e91aab7daa45a68c

Ministry of Health Medical Device Import No. 027848

DHA05602784808

Company Information

United States

Product Details

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

P Devices for radiology

P1560 ultrasonic echo imaging system

Imported from abroad

Dates and Status

Nov 13, 2015

Nov 13, 2025