Chewy Tubes

GUDID 00850036595229

CASCO BAY MOLDING LTD.

Teething device, non-fluid-filled

• Primary Device ID: 00850036595229
• NIH Device Record Key: 62b476c9-bf9e-42cf-ad37-7c37c97f18f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Chewy Tubes
• Version Model Number: Y
• 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	00850036595229 [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: 2025-02-03
• Device Publish Date: 2025-01-24

On-Brand Devices [Chewy Tubes]

• 00850036595281: APCT
• 00850036595274: ADSCT
• 00850036595250: SDR
• 00850036595243: B
• 00850036595236: R
• 00850036595229: Y
• 00850036595212: K
• 00850036595106: KQ2
• 00850036595069: KPP2
• 00850036595052: PQR
• 00850036595045: SS
• 00850036595021: SCG
• 00850036595007: SCR
• 00850036595113: CQ2
• 00850036595083: PQG1
• 00850036595076: PQO1