FDA UDI In Commercial Distribution 🇺🇸 United States

LIAISON PLEX® Respiratory Flex Assay Kit

DI: 00840487101940 · Model: 20-005-322 · LUMINEX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
LIAISON PLEX® Respiratory Flex Assay Kit
Primary DI
00840487101940
Version / Model
20-005-322
Catalog Number
20-005-322
Company Name
LUMINEX CORPORATION
Labeler DUNS
080778937
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-20
Public Version
2
Public Version Date
2026-02-27
Public Version Status
Update
Public Device Record Key
0703a478-e2cf-4b99-86ab-aec6273aae34

Device Description

The LIAISON PLEX® Respiratory Flex (RSP Flex) Assay is a multiplexed qualitative test for the simultaneous in vitro detection and identification of multiple bacterial and viral nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals with clinical signs and symptoms of respiratory tract infection, including SARS-CoV-2.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QOF Multi-target respiratory specimen nucleic acid test including SARS-CoV-2 and other microbial agents

GMDN Terms

Code Name
61527 Multiple-type respiratory pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)

Identifiers

Type ID
Primary 00840487101940

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K233410 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius