RIVERSILK

GUDID 10810020085195

Suture

RIVERPOINT MEDICAL, LLC

Silk suture

• Primary Device ID: 10810020085195
• NIH Device Record Key: 581cc7ec-5d31-4d35-944e-54c52787a730
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RIVERSILK
• Version Model Number: S7772
• 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	00810020085198 [Primary]
GS1	10810020085195 [Package]; Contains: 00810020085198; 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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-02-05
• Device Publish Date: 2020-09-18

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