Restrata Meshed

GUDID 00854258006280

The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.

Acera Surgical Inc

Synthetic wound matrix dressing

• Primary Device ID: 00854258006280
• NIH Device Record Key: c5a877f6-12ed-4909-96d9-436ddddaf130
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Restrata Meshed
• Version Model Number: RMESH-3X3
• Company DUNS: 040631370
• Company Name: Acera Surgical Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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	00854258006280 [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: 2022-04-29
• Device Publish Date: 2022-04-21

On-Brand Devices [Restrata Meshed]

• 00854258006303: The Restrata Wound Matrix is a sterile, single use device intended for use in local management o
• 00854258006297: The Restrata Wound Matrix is a sterile, single use device intended for use in local management o
• 00854258006280: The Restrata Wound Matrix is a sterile, single use device intended for use in local management o
• 00854258006273: The Restrata Wound Matrix is a sterile, single use device intended for use in local management o
• 00854258006266: The Restrata Wound Matrix is a sterile, single use device intended for use in local management o