Romenes clinical multi-standard detector - Taiwan Registration 019598ec37f56c8617225905e48761fb
Access comprehensive regulatory information for Romenes clinical multi-standard detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 019598ec37f56c8617225905e48761fb and manufactured by LUMINEX CORPORATION. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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Device Details
Product Details
The Luminex 200 System can be used with specialized reagents for a variety of xMAP technology-based experimental tests to detect biomolecular reactions on the surface of xMAP microspheres. The system is mainly used for in vitro diagnostics.
A Clinical chemistry and clinical toxicology
A.2570 Clinical Multi-standard Detection System Instrument
import
Dates and Status
Oct 30, 2012
Oct 30, 2027