The COVID
COVID-19 total Ab Control LQ - FIC-COALQ
Device Description
A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of total antibodies to severe acute respiratory syndrome-associated coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, in a clinical specimen.
Environmental Conditions
No Data Available
Device Sizes
No Data Available
Device Sterilization
Device Sterile: False
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: QKO
Device Name: Reagent, Coronavirus Serological
Device Class: N
Physical State: In vitro diagnostic device.
Definition: The qualitative detection of IgM and/or IgG antibodies to coronavirus from human specimens.
Submission Type ID: 8
Review Panel: MI
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: Serological assay.
Life Sustain Support Flag: N
Unclassified Reason: 11
Implant Flag: N
Target Area: Detection and differentiation of IgM and/or IgG antibodies from human specimens.
Regulation Number: N/A
Third Party Flag: N
Medical Specialty: N/A
Device IdentifiersDevice Id: 08809317540917
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A
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