PolyPro

GUDID 10840277407563

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin/fluoropolymer suture, multifilament

• Primary Device ID: 10840277407563
• NIH Device Record Key: 0944ba54-947e-4948-8993-00bc4e2b73c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PolyPro
• Version Model Number: 8557P
• 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	00840277407566 [Primary]
GS1	10840277407563 [Package]; Contains: 00840277407566; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAW: Suture, Nonabsorbable, Synthetic, Polypropylene

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: 2025-01-22
• Device Publish Date: 2025-01-14

On-Brand Devices [PolyPro]

• 10840277406160: Suture
• 10840277407785: Suture
• 10840277407778: Suture
• 10840277407761: Suture
• 10840277407754: Suture
• 10840277407747: Suture
• 10840277407730: Suture
• 10840277407600: Suture
• 10840277407594: Suture
• 10840277407587: Suture
• 10840277407570: Suture
• 10840277407563: Suture
• 10840277407556: Suture
• 10840277407549: Suture
• 10840277407532: Suture