AquaRite Ag Extra CMC

GUDID 07141964666000

DERMARITE INDUSTRIES LLC

Petrolatum woven gauze pad

• Primary Device ID: 07141964666000
• NIH Device Record Key: 8b605c97-9dd4-4806-b1ca-243f499d4928
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AquaRite Ag Extra CMC
• Version Model Number: 46660
• 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	00714196466600 [Package]; Package: [5 Units]; In Commercial Distribution
GS1	07141964666000 [Primary]

FDA Product Code

• NAC: Dressing, Wound, Hydrophilic

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: 2025-06-09
• Device Publish Date: 2025-06-01

On-Brand Devices [AquaRite Ag Extra CMC]

• 07141964666000: 46660
• 00714196464507: 46450