| Primary Device ID | 00880304521131 |
| NIH Device Record Key | 5e8121bc-c9eb-4e41-974f-ecfae7452f7f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STAGEONE SELECT |
| Version Model Number | 431198 |
| Catalog Number | 431198 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | true |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304521131 [Primary] |
| KWL | Prosthesis, hip, hemi-, femoral, metal |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-09-23 |
| Device Publish Date | 2015-10-24 |
| 00880304521995 | 431190 |
| 00880304521254 | 431183 |
| 00880304521247 | 431192 |
| 00880304521230 | 431191 |
| 00880304521179 | 431193 |
| 00880304521162 | 431199 |
| 00880304521155 | 431194 |
| 00880304521148 | 431197 |
| 00880304521131 | 431198 |
| 00880304521124 | 431195 |
| 00880304521117 | 431196 |
| 00880304521100 | 431181 |
| 00880304521094 | 431188 |
| 00880304521087 | 431186 |
| 00880304521070 | 431187 |
| 00880304521063 | 431185 |
| 00880304521056 | 431184 |
| 00880304521032 | 431182 |