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Lumis multi-standard fluorescence analyzer - Taiwan Registration ee1d8d7132aa7a453e98c8936a415d53

Access comprehensive regulatory information for Lumis multi-standard fluorescence analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee1d8d7132aa7a453e98c8936a415d53 and manufactured by LUMINEX CORPORATION. The authorized representative in Taiwan is METEK LAB 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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ee1d8d7132aa7a453e98c8936a415d53
Registration Details
Taiwan FDA Registration: ee1d8d7132aa7a453e98c8936a415d53
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Device Details

Lumis multi-standard fluorescence analyzer
TW: ่ทฏ็ฑณๆ–ฏๅคšๆจ™็š„่žขๅ…‰ๅˆ†ๆžๅ„€
Risk Class 2
Cancelled

Registration Details

ee1d8d7132aa7a453e98c8936a415d53

DHA00602383206

Company Information

United States

Product Details

Multi-standard detection and fluorescence analysis with instrument-specific reagents.

A Clinical chemistry and clinical toxicology

A.2570 Clinical Multi-standard Detection System Instrument

import

Dates and Status

Aug 06, 2012

Aug 06, 2022

Apr 12, 2024

Cancellation Information

Logged out

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