DermaAngel Clear Patch Intensive

GUDID 04719745074530

BENQ MATERIALS CORP.

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

• Primary Device ID: 04719745074530
• NIH Device Record Key: 72ec6abe-5227-432c-bb74-5b7df9f5343e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaAngel Clear Patch Intensive
• Version Model Number: AP-SA151-f
• 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	04719745074530 [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 Intensive]

• 04719745074233: AP-SA1c1-6
• 04719745074035: AP-SA1c1-t
• 04719745074547: AP-SA151-p
• 04719745074530: AP-SA151-f
• 04719745086199: AP-SA151-8
• 04719745074158: AP-SA101-2
• 04719745088827: AP-SA1y1-h
• 04719745088810: AP-SA1l1-f
• 04719745088803: AP-SA1i1-t
• 04719745073793: AP-SA151-6
• 04719745091551: AP-SA1i1-s