Monomid

GUDID 10840277407402

Suture

RIVERPOINT MEDICAL, LLC

Nylon suture, non-bioabsorbable, monofilament

• Primary Device ID: 10840277407402
• NIH Device Record Key: d7f736f3-d779-481e-bdc5-a7de5273a493
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Monomid
• Version Model Number: 945B
• 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	00840277407405 [Primary]
GS1	10840277407402 [Package]; Contains: 00840277407405; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAR: Suture, Nonabsorbable, Synthetic, Polyamide

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 [Monomid]

• 10840277406153: Suture
• 10840277406146: Suture
• 10840277406139: Suture
• 10840277406122: Suture
• 10840277407693: Suture
• 10840277407686: Suture
• 10840277407679: Suture
• 10840277407662: Suture
• 10840277407402: Suture
• 10840277407396: Suture
• 10840277407389: Suture
• 10840277407372: Suture
• 10840277407365: Suture
• 10840277407358: Suture
• 10840277407341: Suture