myEverCup

GUDID B839842F766HT2D0589630

CASCO BAY MOLDING LTD.

Menstrual cup, non-latex, single-use

• Primary Device ID: B839842F766HT2D0589630
• NIH Device Record Key: 11d402b7-c102-41a2-8388-8363857b12ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: myEverCup
• Version Model Number: 3HQAZHE9N842F766HT2D058963
• 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	B839842F766HT2D0589630 [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: 2020-08-07
• Device Publish Date: 2020-07-30

On-Brand Devices [myEverCup]

• B8397QJMD6N2Q2171C34A0: 7KTD9QAT57QJMD6N2Q2171C34A
• B839DMRNTRQE6EDADE6FB0: 2ADMAN735DMRNTRQE6EDADE6FB
• B839CA7ZCG9YCAFA25EDA0: 2AXHQMKBQCA7ZCG9YCAFA25EDA
• B839842F766HT2D0589630: 3HQAZHE9N842F766HT2D058963
• B8394F5BS5GTNE2FDC52C0: 3PNGECWSA4F5BS5GTNE2FDC52C
• B839WBWANSWY6FPTX7PBP0: 6QMAAWMW4WBWANSWY6FPTX7PBP
• B839NZXX6FYD9602885870: 02BEK8T60NZXX6FYD960288587
• B839KZ20F2N9PK2CS8B5H0: 26X0ARWN1KZ20F2N9PK2CS8B5H
• B8390JNDAGCY2094980F40: 4582RS8TV0JNDAGCY2094980F4
• B839W6983X41NCA53893A0: Size 1 Standard with Violet Cleaning Case
• B839B7RW9NMMV783BC3AA0: Size 1 Standard with Orange Cleaning Case