Tentacle Teether

GUDID 00860012961009

CASCO BAY MOLDING LTD.

Teething device, non-fluid-filled

• Primary Device ID: 00860012961009
• NIH Device Record Key: 30ae55ed-791e-4f67-96ca-c3c7017151eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tentacle Teether
• Version Model Number: Tentacle Violet 3.0
• Company DUNS: 604286695
• Company Name: CASCO BAY MOLDING 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860012961009 [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: 2025-12-02
• Device Publish Date: 2025-11-24

On-Brand Devices [Tentacle Teether]

• 00197644411252: Tentacle Violet
• 00860012961009: Tentacle Violet 3.0