SILK

GUDID 10812444021834

SUTURE

RIVERPOINT MEDICAL, LLC

Silk suture, sterile

• Primary Device ID: 10812444021834
• NIH Device Record Key: 42f011fe-8644-4f8d-8aeb-249e2bf337c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SILK
• Version Model Number: S683
• 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: false
• 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	00812444021837 [Primary]
GS1	10812444021834 [Package]; Contains: 00812444021837; 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: 4
• Public Version Date: 2018-10-15
• Device Publish Date: 2015-10-16

On-Brand Devices [SILK]

• 10812444024118: SUTURE
• 10812444021858: SUTURE
• 10812444021841: SUTURE
• 10812444021834: SUTURE
• 10812444021827: SUTURE
• 10812444021810: SUTURE
• 10812444021803: SUTURE
• 10812444021797: SUTURE
• 10812444021780: SUTURE
• 10840277406191: Suture
• 10840277407792: Suture
• 10840277407464: Suture
• 10840277407457: Suture
• 10840277407440: Suture
• 10840277408850: Suture
• 10840277408843: Suture
• 10840277408560: Suture
• 10840277409208: Suture
• 10840277409192: Suture
• 10840277408577: Suture
• 00840277410153: Suture