| Primary Device ID | 00880304491380 |
| NIH Device Record Key | 429d3ec9-6295-4c6c-a0bc-6e4326ca73c3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ACTIVE ARTICULATION HIP SYSTEM |
| Version Model Number | XL-200156 |
| Catalog Number | XL-200156 |
| 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 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 | 00880304491380 [Primary] |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
| OQG | Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented |
| 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 |
| 00880304491434 | XL-200166 |
| 00880304491427 | XL-200164 |
| 00880304491410 | XL-200162 |
| 00880304491403 | XL-200160 |
| 00880304491397 | XL-200158 |
| 00880304491380 | XL-200156 |
| 00880304491373 | XL-200154 |
| 00880304491366 | XL-200152 |
| 00880304491359 | XL-200150 |
| 00880304491342 | XL-200148 |
| 00880304491335 | XL-200146 |
| 00880304491328 | XL-200144 |
| 00880304485136 | EP-200166 |
| 00880304485129 | EP-200164 |
| 00880304485112 | EP-200162 |
| 00880304485105 | EP-200160 |
| 00880304485099 | EP-200158 |
| 00880304485082 | EP-200156 |
| 00880304485075 | EP-200154 |
| 00880304485068 | EP-200152 |
| 00880304485051 | EP-200150 |
| 00880304485044 | EP-200148 |
| 00880304485037 | EP-200146 |
| 00880304485020 | EP-200144 |