Dr. Brown's

GUDID 00072239318829

Watermelon Soothing Teether

HANDI-CRAFT COMPANY

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• Primary Device ID: 00072239318829
• NIH Device Record Key: 903ea714-a8e5-49ec-b179-2b970ba46ca4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dr. Brown's
• Version Model Number: TE106
• Company DUNS: 055872634
• Company Name: HANDI-CRAFT COMPANY
• 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	00072239318829 [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: 2022-12-08
• Device Publish Date: 2022-11-30