Riversilk

GUDID 10840277405538

Suture

RIVERPOINT MEDICAL, LLC

Silk suture

• Primary Device ID: 10840277405538
• NIH Device Record Key: a0b67d49-83c9-436b-896e-d016a4a02c5b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Riversilk
• Version Model Number: S779
• 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	00840277405531 [Primary]
GS1	10840277405538 [Package]; Contains: 00840277405531; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAP: Suture, Nonabsorbable, Silk

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: 2025-01-22
• Device Publish Date: 2025-01-14

On-Brand Devices [Riversilk]

• 10812444026112: SUTURE
• 10812444025863: Suture
• 10812444024545: SUTURE
• 10810020085195: Suture
• 10810020085188: Suture
• 10840277407129: Suture
• 10840277407099: Suture
• 10840277405552: Suture
• 10840277405545: Suture
• 10840277405538: Suture
• 10840277405507: Suture
• 00840277405487: Suture
• 10840277408584: Suture
• 10840277408591: Suture