Riverbond

GUDID 10840277408423

Suture

RIVERPOINT MEDICAL, LLC

Polyester suture, non-bioabsorbable, multifilament

• Primary Device ID: 10840277408423
• NIH Device Record Key: e8faa7fe-4987-4a6a-9b65-3bd0589ed2b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Riverbond
• Version Model Number: PB563
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• 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: true
• Expiration Date: true
• 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
GS1	00840277408426 [Primary]
GS1	10840277408423 [Package]; Contains: 00840277408426; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAS: Suture, Nonabsorbable, Synthetic, Polyester

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: 2025-06-26
• Device Publish Date: 2025-06-18

On-Brand Devices [Riverbond]

• 10812444021865: SUTURE
• 10840277409437: Suture
• 10840277409413: Suture
• 10840277408454: Suture
• 10840277408447: Suture
• 10840277408430: Suture
• 10840277408423: Suture