Nuby

GUDID 40048526069376

LUV N' CARE, LTD.

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: 40048526069376
• NIH Device Record Key: 7946f2a9-838c-4989-b608-1f80c356c43d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nuby
• Version Model Number: 6937
• Company DUNS: 108926288
• Company Name: LUV N' CARE, LTD.
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00048526069378 [Primary]
GS1	40048526069376 [Package]; Contains: 00048526069378; Package: [4 Units]; In Commercial Distribution
GS1	50048526069373 [Package]; Package: [4 Units]; In Commercial Distribution

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: 2021-08-23
• Device Publish Date: 2021-08-13