CorTTape STICK

GUDID 00840277405852

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin/fluoropolymer suture, multifilament

• Primary Device ID: 00840277405852
• NIH Device Record Key: 5de60f09-fca5-4192-8899-41edd6a9b2f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CorTTape STICK
• Version Model Number: HS178
• 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	00840277405852 [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: 2024-11-01
• Device Publish Date: 2024-10-24

Devices Manufactured by RIVERPOINT MEDICAL, LLC

• 00840277411068 - HS Fiber: 2026-02-03 Suture
• 00840277411396 - HS Fiber: 2026-01-21 Blue/White UHMWPE Polyblend Braided Non-Absorbable Suture Tape
• 10840277411409 - HS Fiber: 2026-01-21 White/Blue UHMWPE polyblend braided non-absorbable suture.
• 00840277410023 - ProZip Knotless Implant: 2026-01-14 ProZip Knotless Implant
• 00840277410030 - ProZip Knotless Implant: 2026-01-14 ProZip Knotless Implant
• 10840277410068 - ProZip Knotless Implant: 2026-01-14 ProZip Knotless Implant
• 10840277410075 - ProZip Knotless Implant: 2026-01-14 ProZip Knotless Implant
• 00840277411365 - ApeLoop: 2025-12-17 Suture