CorDx Tyfast

GUDID 10850042559564

CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC

CORETESTS, INC.

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• Primary Device ID: 10850042559564
• NIH Device Record Key: f7c9897e-05e4-44a1-898f-06cfd0227cf8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CorDx Tyfast
• Version Model Number: ACT21002-4
• Company DUNS: 036440919
• Company Name: CORETESTS, INC.
• Device Count: 4
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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	00850042559543 [Unit of Use]
GS1	00850042559567 [Primary]
GS1	10850042559564 [Package]; Contains: 00850042559567; Package: [78 Units]; In Commercial Distribution

FDA Product Code

• QMN: Covid-19 Multi-Analyte Antigen Device

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: 2024-06-21
• Device Publish Date: 2024-06-13

On-Brand Devices [CorDx Tyfast]

• 10850042559656: CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test POC
• 00850042559635: CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test POC
• 10850042559564: CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC
• 10850042559557: CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC
• 10850042559533: CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC
• 00850042559529: CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test OTC