| Primary Device ID | 00880304475922 |
| NIH Device Record Key | 41821a0b-1327-4cb3-b315-c762e1118ba5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MAXFIRE MARXMEN |
| Version Model Number | 900320 |
| Catalog Number | 900320 |
| Company DUNS | 627100159 |
| Company Name | Biomet Sports Medicine, LLC |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304475922 [Primary] |
| JDR | STAPLE, FIXATION, BONE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-05-06 |
| Device Publish Date | 2015-10-24 |
| 00880304475922 | 900320 |
| 00880304475915 | 900321 |