DermaLevin

GUDID 00714196280442

DERMARITE INDUSTRIES LLC

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

• Primary Device ID: 00714196280442
• NIH Device Record Key: 501270a3-c52f-4626-afef-096a28335226
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaLevin
• Version Model Number: 00280E
• 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	00714196280442 [Primary]
GS1	01714196280441 [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 [DermaLevin]

• 00714196285669: 00285E
• 00714196280442: 00280E
• 00714196392206: 00285E
• 00714196392183: 00280E