Alyte™ Y-Mesh Graft Y500

GUDID 10801741016162

Alyte™ Y-Mesh Graft, 5 Pack

C. R. Bard, Inc.

Pelvic organ prolapse surgical mesh, synthetic polymer

• Primary Device ID: 10801741016162
• NIH Device Record Key: 8ad752f1-a241-4c72-964c-ab26307ef2ba
• Commercial Distribution Discontinuation: 2016-12-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Alyte™ Y-Mesh Graft
• Version Model Number: Y500
• Catalog Number: Y500
• Company DUNS: 016898496
• Company Name: C. R. Bard, 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: true
• 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: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741016165 [Primary]
GS1	10801741016162 [Package]; Contains: 00801741016165; Package: CA [5 Units]; Discontinued: 2016-12-31; Not in Commercial Distribution

FDA Product Code

• OTO: Mesh, surgical, synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-09-14

On-Brand Devices [Alyte™ Y-Mesh Graft]

• 10801741016162: Alyte™ Y-Mesh Graft, 5 Pack
• 00801741016158: Alyte™ Y-Mesh Graft