ComfortFoam Border Lite

GUDID 00714196472205

DERMARITE INDUSTRIES LLC

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

• Primary Device ID: 00714196472205
• NIH Device Record Key: cd52bd9a-f323-4633-bf1a-1ee9124d3a3f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ComfortFoam Border Lite
• Version Model Number: 47220
• Company DUNS: 883925562
• Company Name: DERMARITE INDUSTRIES LLC
• Device Count: 10
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	00714196472205 [Primary]
GS1	01714196472204 [Unit of Use]

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: 2020-09-09
• Device Publish Date: 2020-09-01

On-Brand Devices [ComfortFoam Border Lite]

• 00714196474506: 47440
• 00714196473301: 47330
• 00714196472205: 47220
• 00714196390967: 47440
• 00714196390943: 47330
• 00714196390929: 47220