Luminex FLEXMAP 3D - Taiwan Registration 6e571141490c28564983e98d0da1ba24
Access comprehensive regulatory information for Luminex FLEXMAP 3D in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6e571141490c28564983e98d0da1ba24 and manufactured by LUMINEX CORPORATION. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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Device Details
Registration Details
6e571141490c28564983e98d0da1ba24
Ministry of Health Medical Device Import No. 026298
DHA05602629807
Product Details
The Luminex FLEXMAP 3D system is designed to perform a variety of xMAP technology-based laboratory tests to detect biomolecular reactions on the surface of xMAP beads, primarily for in vitro diagnostics.
A Clinical chemistry and clinical toxicology
A2570 Clinical Multi-standard Detection System Instrument
Imported from abroad
Dates and Status
Aug 11, 2014
Aug 11, 2024