Primary Device ID | 00840487101988 |
NIH Device Record Key | aa3a3f0b-3f23-4efa-979e-df96b56b44c5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LIAISON PLEX® Module (Refurbished) |
Version Model Number | CN-0564-01R |
Company DUNS | 965476641 |
Company Name | LUMINEX CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com | |
Phone | +1(512)381-4397 |
support@luminexcorp.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840487101988 [Primary] |
NSU | Instrumentation for clinical multiplex test systems |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-28 |
Device Publish Date | 2024-06-20 |
00840487101865 - LIAISON PLEX Yeast Blood Culture Assay Kit | 2024-10-30 The LIAISON PLEX® Yeast Blood Culture (BCY) Assay is a qualitative nucleic acid multiplex in vitro diagnostic test intended for |
00840487101940 - LIAISON PLEX® Respiratory Flex Assay Kit | 2024-06-28 The LIAISON PLEX® Respiratory Flex (RSP Flex) Assay is a multiplexed qualitative test for the simultaneous in vitro detection a |
00840487101957 - LIAISON PLEX® Chassis | 2024-06-28 The LIAISON PLEX® is an in vitro diagnostic (IVD) platform that performs nucleic acid based tests in clinical laboratories. The |
00840487101964 - LIAISON PLEX® Chassis (Refurbished) | 2024-06-28 The LIAISON PLEX® is an in vitro diagnostic (IVD) platform that performs nucleic acid based tests in clinical laboratories. The |
00840487101971 - LIAISON PLEX® Module | 2024-06-28 The LIAISON PLEX® Module is a component of the LIAISON PLEX® Chassis. When installed in the LIAISON PLEX® Chassis it is capa |
00840487101988 - LIAISON PLEX® Module (Refurbished) | 2024-06-28The LIAISON PLEX® Module is a component of the LIAISON PLEX® Chassis. When installed in the LIAISON PLEX® Chassis it is capable of automated extraction and purification of nucleic acids from multiple sample types as well as automated amplification, array hybridization, and detection of target nucleic acid sequences. (Refurbished) |
00840487101988 - LIAISON PLEX® Module (Refurbished) | 2024-06-28 The LIAISON PLEX® Module is a component of the LIAISON PLEX® Chassis. When installed in the LIAISON PLEX® Chassis it is capa |
00840487101797 - MAGPIX® Drive Fluid PLUS (4PK) | 2022-09-16 The MAGPIX Drive Fluid PLUS serves as the delivery medium that carries the sample to the optics component of the MAGPIX instrume |
00840487101803 - xMAP® Sheath Fluid PLUS | 2022-09-16 Sheath Fluid PLUS is the delivery medium of the sample to the optics component. |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LIAISON PLEX 98062754 not registered Live/Pending |
DIASORIN S.P.A. 2023-06-28 |
LIAISON PLEX 98062754 not registered Live/Pending |
LUMINEX CORPORATION 2023-06-28 |