ARTHROLINK

GUDID 00840277406101

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin/fluoropolymer suture, multifilament

• Primary Device ID: 00840277406101
• NIH Device Record Key: 0ac103d4-c377-4856-80e2-33b0eed18b11
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ARTHROLINK
• Version Model Number: HS1062
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840277406101 [Primary]

FDA Product Code

• GAT: Suture, Nonabsorbable, Synthetic, Polyethylene

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: 2024-11-07
• Device Publish Date: 2024-10-30

On-Brand Devices [ARTHROLINK]

• 00812444026689: SUTURE
• 00812444026672: SUTURE
• 00812444026665: SUTURE
• 00812444026658: HS957
• 00840277406118: Suture
• 00840277406101: Suture
• 00840277406095: Suture
• 00840277406088: Suture
• 00840277406071: Suture
• 00840277406064: Suture
• 00840277406057: Suture
• 00840277406040: Suture
• 00840277406033: Suture
• 00840277406026: Suture
• 00840277406019: Suture
• 00840277406002: Suture
• 00840277405999: Suture
• 00840277405982: Suture
• 00840277405975: Suture
• 00840277405968: Suture