OVACUP

GUDID B8393XPM7HDFHF29FC4800

OVACUP Egg S Engraved Menstrual Cup

CASCO BAY MOLDING LTD.

Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable

• Primary Device ID: B8393XPM7HDFHF29FC4800
• NIH Device Record Key: fbc205ff-7774-4574-85f5-35b9c9c502d0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OVACUP
• Version Model Number: Mid 42 Bell
• 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
HIBCC	B8393XPM7HDFHF29FC4800 [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: 2020-10-29
• Device Publish Date: 2020-10-21

On-Brand Devices [OVACUP]

• B839R8Y3BK0VZE2CE39560: OVACUP Egg L Engraved
• B8393XPM7HDFHF29FC4800: OVACUP Egg S Engraved Menstrual Cup