Be Girl

GUDID 00816132022830

Model 1 Standard

CASCO BAY MOLDING LTD.

Menstrual cup, non-latex, reusable

• Primary Device ID: 00816132022830
• NIH Device Record Key: e0b4e97f-a902-4448-aa4d-a703f55842b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Be Girl
• Version Model Number: Model 1 Standard
• 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	00816132022830 [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: 2020-10-05
• Device Publish Date: 2020-09-25

Devices Manufactured by CASCO BAY MOLDING LTD.

• 00860012961009 - Tentacle Teether: 2025-12-02
• 00860013832001 - Selaviera Cup: 2025-06-26 Selaviera Menstrual Cup small
• 00860013832018 - Selaviera Cup: 2025-06-26 Selaviera Menstrual Cup medium
• 00860013832025 - Selaviera Cup: 2025-06-26 Selaviera Menstrual Cup large
• 00850066493052 - Casco Cup: 2025-02-17
• 00850036595076 - Chewy Tubes: 2025-02-04
• 00850036595083 - Chewy Tubes: 2025-02-04
• 00850036595113 - Chewy Tubes: 2025-02-04