CascoCup

GUDID B839T2YW19J3Y4B03F5980

CASCO BAY MOLDING LTD.

Menstrual cup, non-latex, single-use

• Primary Device ID: B839T2YW19J3Y4B03F5980
• NIH Device Record Key: 3104173f-c6c0-4777-a037-ff53d349304c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CascoCup
• Version Model Number: 5YHAR288BT2YW19J3Y4B03F598
• 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	B839T2YW19J3Y4B03F5980 [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: 2020-07-31
• Device Publish Date: 2020-07-23

On-Brand Devices [CascoCup]

• B839T2YW19J3Y4B03F5980: 5YHAR288BT2YW19J3Y4B03F598
• B839QG1A3R6BH9272A3170: 5RD6X9Y56QG1A3R6BH9272A317
• B8393P0NW4YVNYKYEV6DS0: 4AE4SDNJE3P0NW4YVNYKYEV6DS