FORA

GUDID 00816042014109

Uric Acid Test System

FORA CARE INC.

Uric acid monitoring system IVD, home-use

• Primary Device ID: 00816042014109
• NIH Device Record Key: b6f2a796-69d2-4ad0-85d1-92b70cdac7e3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FORA
• Version Model Number: 6 Connect
• Company DUNS: 004340807
• Company Name: FORA CARE 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: false
• Lot Batch: true
• Serial Number: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816042014109 [Primary]

FDA Product Code

• LFQ: Acid, Uric, Acid Reduction Of Ferric Ion

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: 2023-07-04
• Device Publish Date: 2023-06-26

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