Ingenuity

GUDID 00074451168824

KIDS II, INC.

Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled Teething device, fluid-filled

• Primary Device ID: 00074451168824
• NIH Device Record Key: 519b7428-99d8-4364-8259-ad2c53a976b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ingenuity
• Version Model Number: 16882
• Company DUNS: 063536098
• Company Name: KIDS II, 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: false
• 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	00074451168824 [Primary]

FDA Product Code

• KKO: Ring, Teething, 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: 2023-05-08
• Device Publish Date: 2023-04-28

On-Brand Devices [Ingenuity]

• 00074451168824: 16882
• 00074451168817: 16881