ARTHROLINK

GUDID 00812444026672

SUTURE

RIVERPOINT MEDICAL, LLC

Polyolefin suture, multifilament

• Primary Device ID: 00812444026672
• NIH Device Record Key: e8658bf8-32ce-42be-bcb4-f382809e3656
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ARTHROLINK
• Version Model Number: HS958
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812444026672 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-02-07
• Device Publish Date: 2017-07-20

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