Lunable

GUDID 00860012792801

Menstrual Disc

Yayoi FemTech Inc.

Menstrual cup/disc, non-latex, reusable

• Primary Device ID: 00860012792801
• NIH Device Record Key: 73071f13-42e7-4f26-af84-87e86f342444
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lunable
• Version Model Number: 1
• Company DUNS: 243327022
• Company Name: Yayoi FemTech Inc.
• 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: false
• 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	00860012792801 [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: 2025-09-10
• Device Publish Date: 2025-09-02