MiroTract Wound Matrix

GUDID 00857072005460

Wound Matrix

REPRISE BIOMEDICAL, INC.

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• Primary Device ID: 00857072005460
• NIH Device Record Key: cd1104f1-479b-46f1-ad0c-eb72bda3f2f8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MiroTract Wound Matrix
• Version Model Number: 5020
• Company DUNS: 043611421
• Company Name: REPRISE BIOMEDICAL, 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: 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

Customer Support Contacts

• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com
• Phone: 952-377-8238
• Email: customerservice@reprisebio.com

Device Dimensions

• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter
• Length: 5 Centimeter
• Outer Diameter: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857072005460 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K231614

FDA Product Code

• KGN: Wound Dressing With Animal-Derived Material(S)

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: 2023-12-29
• Device Publish Date: 2023-12-21

On-Brand Devices [MiroTract Wound Matrix]

• 00857072005484: Wound Matrix
• 00857072005477: Wound Matrix
• 00857072005460: Wound Matrix
• 00857072005453: Wound Matrix