Humes

GUDID 00860011787303

CASCO BAY MOLDING LTD.

Menstrual cup, non-latex, reusable

• Primary Device ID: 00860011787303
• NIH Device Record Key: 3dba68fc-e849-4806-a7fd-aab3af4f2313
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Humes
• Version Model Number: Size 1
• 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	00860011787303 [Primary]

FDA Product Code

• HHE: Cup, Menstrual

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: 2024-05-24
• Device Publish Date: 2024-05-16

On-Brand Devices [Humes]

• 00197644760619: Disc
• 00197644645664: Size 2
• 00197644014033: Size 1
• 00860011787327: Disc
• 00860011787310: Size 2
• 00860011787303: Size 1