| Primary Device ID | 00887868106552 |
| NIH Device Record Key | d895959e-6f6c-495e-ba10-685693750bc3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OSSEOTI RECONSTRUCTIVE SYSTEM |
| Version Model Number | 110003815 |
| Catalog Number | 110003815 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868106552 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
| 00887868130939 | 110003784 |
| 00887868130922 | 110003772 |
| 00887868130915 | 110003760 |
| 00887868106590 | 110003831 |
| 00887868106583 | 110003827 |
| 00887868106576 | 110003821 |
| 00887868106569 | 110003819 |
| 00887868106552 | 110003815 |
| 00887868106545 | 110003809 |
| 00887868106538 | 110003807 |
| 00887868106521 | 110003803 |
| 00887868106514 | 110003797 |
| 00887868106507 | 110003794 |
| 00887868106491 | 110003790 |
| 00887868106484 | 110003786 |
| 00887868106477 | 110003782 |
| 00887868106460 | 110003778 |
| 00887868106453 | 110003774 |
| 00887868106446 | 110003770 |
| 00887868106439 | 110003766 |
| 00887868106422 | 110003762 |