Arthrex DX Reinforcement Matrix ABS-30002S

GUDID 00812337020022

DSM BIOMEDICAL, INC.

Multi-purpose surgical mesh, collagen, bioabsorbable

• Primary Device ID: 00812337020022
• NIH Device Record Key: 394f4e16-5d7b-4195-abac-a54caab743e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arthrex DX Reinforcement Matrix
• Version Model Number: 30030-02
• Catalog Number: ABS-30002S
• Company DUNS: 131107757
• Company Name: DSM BIOMEDICAL, 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 Dimensions

• Width: 6 Centimeter
• Width: 6 Centimeter
• Width: 6 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter
• Length: 8 Centimeter
• Width: 6 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812337020022 [Primary]

FDA Product Code

• OWY: Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-13
• Device Publish Date: 2015-09-04

On-Brand Devices [Arthrex DX Reinforcement Matrix]

• 00812337020022: 30030-02
• 00812337020015: 30030-01
• M263ABS30002: 30030-02
• M263ABS30001: 30030-01