AdVance™ XP 720163-03

GUDID 00191506003999

Male Sling System

BOSTON SCIENTIFIC CORPORATION

Stress urinary incontinence surgical mesh, male

• Primary Device ID: 00191506003999
• NIH Device Record Key: 604cc6a9-9a75-4588-b560-1d23f79b5d73
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AdVance™ XP
• Version Model Number: 720163-03
• Catalog Number: 720163-03
• Company DUNS: 021717889
• Company Name: BOSTON SCIENTIFIC CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00191506003999 [Primary]

FDA Product Code

• OTM: Mesh, surgical, for stress urinary incontinence, male

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-03-29
• Device Publish Date: 2022-03-21

On-Brand Devices [AdVance™ XP]

• 00878953005560: Male Sling System
• 00191506003999: Male Sling System