| Primary Device ID | 00880304082991 |
| NIH Device Record Key | 1a32a5ca-cd70-43ad-a798-6aedb71af9e3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Modular Arthrodesis Nail |
| Version Model Number | CP260602 |
| Catalog Number | CP260602 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | 00880304082991 [Primary] |
| HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-05-11 |
| Device Publish Date | 2015-11-30 |
| 00880304083073 | CP260610 |
| 00880304083066 | CP260609 |
| 00880304083059 | CP260608 |
| 00880304083042 | CP260607 |
| 00880304083035 | CP260606 |
| 00880304083028 | CP260605 |
| 00880304083011 | CP260604 |
| 00880304083004 | CP260603 |
| 00880304082991 | CP260602 |
| 00880304082984 | CP260601 |
| 00880304082977 | CP260600 |