| Primary Device ID | M263ABS30001 | 
| NIH Device Record Key | 0a417dc0-b430-4771-b30c-a93f33c3e275 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Arthrex DX Reinforcement Matrix | 
| Version Model Number | 30030-01 | 
| Catalog Number | ABS-30001S | 
| 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 | 
| Length | 5 Centimeter | 
| Width | 5 Centimeter | 
| Length | 5 Centimeter | 
| Width | 5 Centimeter | 
| Length | 5 Centimeter | 
| Width | 5 Centimeter | 
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| Length | 5 Centimeter | 
| Width | 5 Centimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| HIBCC | M263ABS30001 [Primary] | 
| OWY | Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 4 | 
| Public Version Date | 2022-06-10 | 
| Device Publish Date | 2015-09-04 | 
| 00812337020022 | 30030-02 | 
| 00812337020015 | 30030-01 | 
| M263ABS30002 | 30030-02 | 
| M263ABS30001 | 30030-01 |