Colink Standard CL

GUDID 00812444028416

Does not contain

RIVERPOINT MEDICAL, LLC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00812444028416
• NIH Device Record Key: c5d8ae68-6b8c-4bc9-8f13-7ef36cd15fac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Colink Standard CL
• Version Model Number: TEK-OBCL-20
• 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	00812444028416 [Primary]

FDA Product Code

• MBI: Fastener, Fixation, Nondegradable, Soft Tissue

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: 2019-03-21
• Device Publish Date: 2018-07-03

On-Brand Devices [Colink Standard CL]

• 00812444028577: Suture Button Loop
• 00812444028560: Suture Button Loop
• 00812444028553: Suture Button Loop
• 00812444028546: Suture Button Loop
• 00812444028539: Suture Button Loop
• 00812444028522: Suture Button Loop
• 00812444028515: Suture Button Loop
• 00812444028508: Suture Button Loop
• 00812444028416: Does not contain
• 00812444028409: Suture Button Loop
• 00812444028850: Suture button loop