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Luminex 200 - Taiwan Registration 465949174653585cb78e4f9e566002ce

Access comprehensive regulatory information for Luminex 200 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 465949174653585cb78e4f9e566002ce and manufactured by LUMINEX CORPORATION. The authorized representative in Taiwan is METEK LAB INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LUMINEX CORPORATION, and 1 recent registrations in the same category. 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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465949174653585cb78e4f9e566002ce
Registration Details
Taiwan FDA Registration: 465949174653585cb78e4f9e566002ce
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Device Details

Luminex 200
TW: "่ทฏ็ฑณๆ–ฏ"ๅคšๆจ™็š„่žขๅ…‰ๅˆ†ๆžๅ„€
Risk Class 2
MD

Registration Details

465949174653585cb78e4f9e566002ce

Ministry of Health Medical Device Import No. 030518

DHA05603051800

Company Information

United States

Product Details

The Lumis multi-standard fluorescence analyzer is a multiplex analysis system for the measurement and classification of multiplex targets in vitro diagnosis of clinical specimens. The instrument uses specialized reagents for multi-standard detection to aid diagnosis. The device includes a signal reading device, raw data storage device, data acquisition software and data processing software.

A Clinical chemistry and clinical toxicology

A2570 Clinical Multi-standard Detection System Instrument

Imported from abroad

Dates and Status

Mar 12, 2018

Mar 12, 2023

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