GenaCheck COVID-19 / Flu Rapid Self-Test Kit

GUDID 00810143620085

Genabio Diagnostics Inc.

SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical

• Primary Device ID: 00810143620085
• NIH Device Record Key: 3fefcf0c-7cc2-40d2-abd7-54992613fddc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GenaCheck COVID-19 / Flu Rapid Self-Test Kit
• Version Model Number: RA9-E02401
• Company DUNS: 118586095
• Company Name: Genabio Diagnostics Inc.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810143620085 [Primary]

FDA Product Code

• QKP: Coronavirus Antigen Detection Test System.

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-16
• Device Publish Date: 2023-10-06

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