Bright Starts

GUDID 00074451101128

KIDS II, INC.

Teething device, fluid-filled

• Primary Device ID: 00074451101128
• NIH Device Record Key: a30fcbc8-a41f-4188-a5ec-61f032370eb3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bright Starts
• Version Model Number: 10112
• 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	00074451101128 [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: 2019-08-28
• Device Publish Date: 2019-08-20

On-Brand Devices [Bright Starts]

• 00074451117983: 11798
• 00074451117211: 11721
• 00074451102194: 10219
• 00074451102040: 10204
• 00074451090637: 9063
• 00074451088368: 8836
• 00074451086739: 8673
• 00074451081956: 8195
• 00074451118294: 11829
• 00074451101128: 10112