DermaAngel Acne patch

GUDID 04719745027055

No description.

BENQ MATERIALS CORP.

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

• Primary Device ID: 04719745027055
• NIH Device Record Key: 9c3b56d3-172b-4c17-99a6-eaa6928c614d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DermaAngel Acne patch
• Version Model Number: AP-362-c
• 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	04719745027055 [Primary]
GS1	04719745027079 [Package]; Package: [150 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 Acne patch]

• 04719745072628: No description.
• 04719745053580: No description.
• 04719745053085: No description.
• 04719745053054: No description.
• 04719745040429: No description.
• 04719745027055: No description.