ComfortFoam

GUDID 00714196390707

DERMARITE INDUSTRIES LLC

Exudate-absorbent dressing, non-gel, non-antimicrobial

• Primary Device ID: 00714196390707
• NIH Device Record Key: ed5d5942-8031-472e-bdfe-b39ea54c5ff1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ComfortFoam
• Version Model Number: 44880
• Company DUNS: 883925562
• Company Name: DERMARITE INDUSTRIES LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00714196390707 [Primary]

FDA Product Code

• NAD: Dressing, Wound, Occlusive

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: 2021-09-17
• Device Publish Date: 2021-09-09

On-Brand Devices [ComfortFoam]

• 00714196448804: 44880
• 00714196446800: 44680
• 00714196444806: 44480
• 00714196443304: 44330
• 00714196442208: 44220
• 00714196316660: 00316E
• 00714196315441: 00315E
• 00714196044457: 44450
• 00714196390707: 44880
• 00714196390684: 44680
• 00714196390660: 44480
• 00714196390646: 44450
• 00714196390622: 44330
• 00714196390608: 44220
• 00714196390585: 00316E
• 00714196390561: 00315E