PERMACORD™ Stiffened Suture

GUDID 00840277402202

Size 2 Stiffened Suture Blue, UHMWPE Non-absorbable Suture

RIVERPOINT MEDICAL, LLC

Polyolefin/fluoropolymer suture, multifilament

• Primary Device ID: 00840277402202
• NIH Device Record Key: d8a09be4-7d58-41be-9423-8c531f8c30ff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PERMACORD™ Stiffened Suture
• Version Model Number: 280611
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• Device Count: 6
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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	00840277402202 [Unit of Use]
GS1	10840277402209 [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: 2025-05-06
• Device Publish Date: 2025-04-28

On-Brand Devices [PERMACORD™ Stiffened Suture]

• 00840277402226: Size 2 Stiffened Suture White/Blue, UHMWPE Non-absorbable Suture
• 00840277402202: Size 2 Stiffened Suture Blue, UHMWPE Non-absorbable Suture
• 00840277402219: Size 2 Stiffened Suture White/Blue, UHMWPE Non-absorbable Suture
• 00840277402196: Size 2 Stiffened Suture Blue, UHMWPE Non-absorbable Suture