VeriQuick

GUDID 00049696739344

MULTI-DRUG URINE TEST DIP CARD

FOURSTAR GROUP INC.

Benzodiazepine group IVD, kit, enzyme immunoassay (EIA)

• Primary Device ID: 00049696739344
• NIH Device Record Key: f55e24b7-7a1b-426a-8a05-4f96f517e9ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VeriQuick
• Version Model Number: 11012637M
• Company DUNS: 656091279
• Company Name: FOURSTAR GROUP INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00049696739344 [Primary]

FDA Product Code

• JXM: Enzyme Immunoassay, Benzodiazepine

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: 2021-08-03
• Device Publish Date: 2021-07-26

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