Phoenix Surgical Wound Matrix Fenestrated

GUDID 00852513007423

NANOFIBER SOLUTIONS, INC.

Synthetic nanofiber barrier dressing

• Primary Device ID: 00852513007423
• NIH Device Record Key: 45652df4-b48e-46f6-b50d-95d2a341c669
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Phoenix Surgical Wound Matrix Fenestrated
• Version Model Number: FG-0056
• Company DUNS: 830384223
• Company Name: NANOFIBER SOLUTIONS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00852513007423 [Primary]

FDA Product Code

• FRO: Dressing, Wound, Drug

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-25
• Device Publish Date: 2025-04-17

On-Brand Devices [Phoenix Surgical Wound Matrix Fenestrated]

• 00852513007324: FG-0052
• 00852513007003: FG-0051
• 00852513007430: FG-0057
• 00852513007423: FG-0056
• 00852513007416: FG-0055
• 00852513007409: FG-0054
• 00852513007393: FG-0053