DermaPrep Skin Prep Pads

GUDID 00714196392220

DERMARITE INDUSTRIES LLC

Synthetic-polymer liquid barrier dressing, non-sterile

• Primary Device ID: 00714196392220
• NIH Device Record Key: 632c5f79-1185-4187-b059-0fe99f009ecc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaPrep Skin Prep Pads
• Version Model Number: 81050
• 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	00714196392220 [Primary]

FDA Product Code

• NEC: Bandage, Liquid, Skin Protectant

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 [DermaPrep Skin Prep Pads]

• 00714196810502: 81050
• 00714196392220: 81050