DermaAngel Clear Patch Original

GUDID 04719745077593

BENQ MATERIALS CORP.

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

• Primary Device ID: 04719745077593
• NIH Device Record Key: f58ecb33-7a6b-405d-a0a9-0c8c8e3e36f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaAngel Clear Patch Original
• Version Model Number: AP-391-8
• Company DUNS: 657476292
• Company Name: BENQ MATERIALS CORP.
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04719745077593 [Primary]

FDA Product Code

• NAC: Dressing, Wound, Hydrophilic

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: 2023-10-19
• Device Publish Date: 2023-10-11

On-Brand Devices [DermaAngel Clear Patch Original]

• 04719745077609: AP-391-j
• 04719745077593: AP-391-8
• 04719745077586: AP-361-8
• 04719745077579: AP-361-5
• 04719745077562: AP-361-c
• 04719745079535: AP-331-5
• 04719745086168: AP-361-4
• 04719745053450: AP-361-3