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“Luminex”ARIES System - Taiwan Registration fd34103cc2050a10ad0a74b6771414cb

Access comprehensive regulatory information for “Luminex”ARIES System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd34103cc2050a10ad0a74b6771414cb and manufactured by LUMINEX CORPORATION. The authorized representative in Taiwan is REFERENCE TECHNOLOGY LIMITED COMPANY.

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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fd34103cc2050a10ad0a74b6771414cb
Registration Details
Taiwan FDA Registration: fd34103cc2050a10ad0a74b6771414cb
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Device Details

“Luminex”ARIES System
TW: “路明克斯”愛維思即時偵測PCR分析儀
Risk Class 2
MD
Cancelled

Registration Details

fd34103cc2050a10ad0a74b6771414cb

Ministry of Health Medical Device Import No. 030539

DHA05603053905

Company Information

United States

Product Details

A Clinical chemistry and clinical toxicology

A2570 Clinical Multi-standard Detection System Instrument

Imported from abroad

Dates and Status

Apr 19, 2018

Apr 19, 2023

Nov 28, 2022

Cancellation Information

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