NUMI

GUDID 00810146467182

Quest USA Corp.

Teething device, non-fluid-filled

• Primary Device ID: 00810146467182
• NIH Device Record Key: 4059857f-26bc-4554-8baa-a3a2ddc3c18f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NUMI
• Version Model Number: NU70001
• Company DUNS: 079869689
• Company Name: Quest USA Corp.
• 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: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00810146467182 [Primary]

FDA Product Code

• MEF: Ring, Teething, Non-Fluid Filled

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: 2024-08-09
• Device Publish Date: 2024-08-01

On-Brand Devices [NUMI]

• 00810146468929: NU70000
• 00810146467182: NU70001