VeriQuick

GUDID 00049696736671

Ovulation Predictor

FOURSTAR GROUP INC.

Luteinizing hormone (LH) IVD, kit, immunochromatographic test (ICT), rapid

• Primary Device ID: 00049696736671
• NIH Device Record Key: 7ca447b5-052b-48e3-8d39-ec9af8a631e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VeriQuick
• Version Model Number: 11013002
• Company DUNS: 656091279
• Company Name: FOURSTAR GROUP 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00049696736671 [Primary]

FDA Product Code

• NGE: Test, Luteinizing Hormone (Lh), Over The Counter

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: 2021-02-17
• Device Publish Date: 2021-02-09

On-Brand Devices [VeriQuick]

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• 00049696609531: 171444
• 00049696736671: Ovulation Predictor
• 00049696736657: Pregnancy Test
• 00004969673664: At Home Marijuana Test Kit
• 00049696736664: At Home Marijuana Test Kit
• 00049696737845: 11012637
• 00049696737838: 11012450S
• 00049696737739: 11012450MB
• 00049696128032: PREGNANCY TEST 2CT
• 00049696739344: MULTI-DRUG URINE TEST DIP CARD
• 00049696708319: AT HOME MULTI-DRUG TEST
• 00049696719018: Pregnancy Test
• 00049696712675: At Home Marijuana Drug Test