Monoswift

GUDID 10840277407426

Suture

RIVERPOINT MEDICAL, LLC

Polyester suture, bioabsorbable, monofilament, non-antimicrobial

• Primary Device ID: 10840277407426
• NIH Device Record Key: 3333d1b4-e324-4cc0-9900-979fe498296f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Monoswift
• Version Model Number: L494
• 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	00840277407429 [Primary]
GS1	10840277407426 [Package]; Contains: 00840277407429; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAM: Suture, Absorbable, Synthetic, Polyglycolic Acid

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 [Monoswift]

• 10840277406184: Suture
• 10840277406177: Suture
• 10840277407723: Suture
• 10840277407716: Suture
• 10840277407709: Suture
• 10840277407433: Suture
• 10840277407426: Suture
• 10840277407419: Suture
• 10840277408836: Suture
• 10840277408829: Suture
• 10840277408812: Suture
• 10840277409161: Suture
• 10840277409154: Suture