DermaAngel Active Patch Intensive

GUDID 04719745108549

No description.

BENQ MATERIALS CORP.

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

• Primary Device ID: 04719745108549
• NIH Device Record Key: b6a087dc-5beb-4bd4-831a-86d8826442e6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaAngel Active 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	04719745108549 [Primary]
GS1	04719745108594 [Package]; Package: [51 Units]; In Commercial Distribution

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: 2022-09-29
• Device Publish Date: 2022-09-21

On-Brand Devices [DermaAngel Active Patch Intensive]

• 04719745108556: No description.
• 04719745108549: No description.