| Primary Device ID | 00887868355905 |
| NIH Device Record Key | cfd986e4-dbb0-4206-b09f-d14f885f87ff |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | G7® OsseoTi® Acetabular Shell |
| Version Model Number | 110010246 |
| Catalog Number | 110010246 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868355905 [Primary] |
| OQI | Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-18 |
| Device Publish Date | 2020-05-08 |
| 00887868356162 | 110010278 |
| 00887868356155 | 110010277 |
| 00887868356148 | 110010276 |
| 00887868356131 | 110010275 |
| 00887868356124 | 110010274 |
| 00887868356117 | 110010273 |
| 00887868356100 | 110010272 |
| 00887868356094 | 110010271 |
| 00887868356087 | 110010270 |
| 00887868356070 | 110010269 |
| 00887868356063 | 110010268 |
| 00887868356056 | 110010267 |
| 00887868356049 | 110010266 |
| 00887868356032 | 110010265 |
| 00887868356025 | 110010264 |
| 00887868356018 | 110010263 |
| 00887868356001 | 110010262 |
| 00887868355998 | 110010261 |
| 00887868355981 | 110010260 |
| 00887868355974 | 110010259 |
| 00887868355967 | 110010252 |
| 00887868355950 | 110010251 |
| 00887868355943 | 110010250 |
| 00887868355936 | 110010249 |
| 00887868355929 | 110010248 |
| 00887868355912 | 110010247 |
| 00887868355905 | 110010246 |
| 00887868355899 | 110010245 |
| 00887868355882 | 110010244 |
| 00887868355875 | 110010243 |
| 00887868355868 | 110010242 |
| 00887868355851 | 110010241 |
| 00887868355844 | 110010240 |