FemCap 70-399-22

GUDID 00863008000102

FemCap™ is indicated for use by women of child-bearing age who desire a barrier device to prevent or postpone pregnancy.

FEMCAP, INC.

Contraceptive cervical cap, reusable

• Primary Device ID: 00863008000102
• NIH Device Record Key: 5cd92fc8-e41d-4ece-adb1-10df246c9e34
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FemCap
• Version Model Number: 22 mm small
• Catalog Number: 70-399-22
• Company DUNS: 140036166
• Company Name: FEMCAP, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 858-481-8837
• Email: femcap@yahoo.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00863008000102 [Primary]

FDA Product Code

• LLQ: Cap, Cervical, Contraceptive

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-04-15

On-Brand Devices [FemCap]

• 00863008000126: FemCap™ is indicated for use by women of child-bearing age who desire a barrier device to prev
• 00863008000119: FemCap™ is indicated for use by women of child-bearing age who desire a barrier device to prev
• 00863008000102: FemCap™ is indicated for use by women of child-bearing age who desire a barrier device to prev