UnnaRite w/ Zinc Healogics by DermaRite

GUDID 00714196939715

DERMARITE INDUSTRIES LLC

Compression bandaging kit

• Primary Device ID: 00714196939715
• NIH Device Record Key: 5021b9c0-fcf8-4e93-9627-58471e443019
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UnnaRite w/ Zinc Healogics by DermaRite
• Version Model Number: 93971
• 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	00714196939715 [Primary]

FDA Product Code

• NEC: Bandage, Liquid, Skin Protectant

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

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 [UnnaRite w/ Zinc Healogics by DermaRite]

• 00714196939722: 93972
• 00714196939715: 93971