| Primary Device ID | 00887868446344 |
| NIH Device Record Key | 8e910a76-7b83-42e5-838b-784fe432d87f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DVR® CROSSLOCK |
| Version Model Number | 131824051 |
| Catalog Number | 131824051 |
| 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 | 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 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 | 00887868446344 [Primary] |
| LXT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-27 |
| Device Publish Date | 2020-07-17 |
| 00887868446351 | 131825051 |
| 00887868446344 | 131824051 |
| 00887868446337 | 1318-23-051 |
| 00887868446320 | 1318-22-176 |
| 00887868446313 | 1318-22-126 |
| 00887868446306 | 1318-22-091 |
| 00887868446290 | 1318-22-061 |
| 00887868446283 | 1318-22-051 |
| 00887868446276 | 1318-22-041 |
| 00887868446269 | 1318-21-051 |
| 00887868446252 | 1318-21-041 |
| 00887868446245 | 1318-20-051 |
| 00887868446238 | 131815051 |
| 00887868446221 | 131814051 |
| 00887868446214 | 1318-13-051 |
| 00887868446207 | 1318-12-176 |
| 00887868446191 | 1318-12-126 |
| 00887868446184 | 1318-12-091 |
| 00887868446160 | 1318-12-061 |
| 00887868446153 | 1318-12-051 |
| 00887868446146 | 1318-12-041 |
| 00887868446139 | 1318-11-051 |
| 00887868446122 | 1318-11-041 |
| 00887868446115 | 1318-10-051 |
| 00880304805811 | 231200006 |