ScarAway Silicone Clear Scar Sheets

GUDID 00358962203404

ScarAway Silicone Clear Scar Sheets, 10ct AP

Alliance Pharma Inc.

Scar-management dressing, reusable

• Primary Device ID: 00358962203404
• NIH Device Record Key: af05d6a4-9f55-4dc3-bc5a-6e20a30cbbe6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ScarAway Silicone Clear Scar Sheets
• Version Model Number: Lot Code
• Company DUNS: 081138954
• Company Name: Alliance Pharma Inc.
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00358962203404 [Primary]

FDA Product Code

• MDA: Elastomer, Silicone, For Scar Management

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: 2024-05-01
• Device Publish Date: 2024-04-23

On-Brand Devices [ScarAway Silicone Clear Scar Sheets]

• 00358962203404: ScarAway Silicone Clear Scar Sheets, 10ct AP
• 00358962203305: ScarAway Silicone Clear Scar Sheets, 6ct AP