Castle Teething Ring

GUDID 00850036799573

Water Filled Rattle

Supermouth LLC

Teething device, fluid-filled

• Primary Device ID: 00850036799573
• NIH Device Record Key: a2322cb5-9e5b-4ef0-a87f-0da64326eb07
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Castle Teething Ring
• Version Model Number: 501101001
• Company DUNS: 049384038
• Company Name: Supermouth LLC
• 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: true
• 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	00850036799573 [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: 2024-06-10
• Device Publish Date: 2024-06-01

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