DermaFoam

GUDID 00714196391889

DERMARITE INDUSTRIES LLC

Wound-nonadherent dressing, absorbent, non-antimicrobial

• Primary Device ID: 00714196391889
• NIH Device Record Key: 31cc2629-c9ac-4de0-9441-5df070efc578
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaFoam
• Version Model Number: 00293E
• 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	00714196391889 [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 [DermaFoam]

• 00714196293015: 00293E
• 00714196292667: 00292E
• 00714196291448: 00291E
• 00714196290229: 00290E
• 00714196391889: 00293E
• 00714196391865: 00292E
• 00714196391841: 00291E
• 00714196391827: 00290E