MonoTex

GUDID 10840277402698

Suture

RIVERPOINT MEDICAL, LLC

Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament

• Primary Device ID: 10840277402698
• NIH Device Record Key: f9ba6bc5-3b74-4695-8d80-1bdd67bbba6f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MonoTex
• Version Model Number: T8624
• 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	00840277402691 [Primary]
GS1	10840277402698 [Package]; Contains: 00840277402691; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• NBY: Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene

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: 2023-08-17
• Device Publish Date: 2023-08-09

On-Brand Devices [MonoTex]

• 10812444026419: SUTURE
• 10812444025139: SUTURE
• 10812444023814: SUTURE
• 10812444022312: SUTURE
• 10812444020660: SUTURE
• 10812444020653: SUTURE
• 10812444020646: SUTURE
• 10812444020639: SUTURE
• 10812444020622: SUTURE
• 10812444020615: SUTURE
• 10812444020608: SUTURE
• 10812444020592: SUTURE
• 10812444020585: SUTURE
• 10812444020578: SUTURE
• 10812444020561: SUTURE
• 10812444020554: SUTURE
• 10812444020547: SUTURE
• 10812444020530: SUTURE
• 10812444020523: SUTURE
• 10812444020516: SUTURE
• 10812444020509: SUTURE
• 10810020086697: Suture
• 10812444029359: Suture
• 10812444029342: Suture
• 10810020085034: Suture
• 10810020087830: Suture
• 10810020087823: Suture
• 10840277402698: Suture