| Primary Device ID | 00880304593176 |
| NIH Device Record Key | 08d5edb4-19e7-4a2b-8e1a-3b326b628b96 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RINGLOC+ HIP SYSTEM |
| Version Model Number | 16-116064 |
| Catalog Number | 16-116064 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304593176 [Primary] |
| KWA | Prosthesis, hip, semi-constrained (metal uncemented acetabular component) |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, 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 |
| 00880304593268 | 16-116082 |
| 00880304593251 | 16-116080 |
| 00880304593244 | 16-116078 |
| 00880304593237 | 16-116076 |
| 00880304593220 | 16-116074 |
| 00880304593213 | 16-116072 |
| 00880304593206 | 16-116070 |
| 00880304593190 | 16-116068 |
| 00880304593183 | 16-116066 |
| 00880304593176 | 16-116064 |
| 00880304593169 | 16-116062 |
| 00880304593152 | 16-116060 |
| 00880304593145 | 16-116058 |
| 00880304593138 | 16-116056 |
| 00880304593121 | 16-116054 |
| 00880304593114 | 16-116052 |
| 00880304593091 | 16-116050 |
| 00880304593084 | 16-116048 |
| 00880304593077 | 16-116046 |
| 00880304593060 | 16-116044 |
| 00880304593053 | 16-116042 |
| 00880304593046 | 16-116040 |
| 00880304593039 | 16-104180 |
| 00880304593022 | 16-104178 |
| 00880304593015 | 16-104176 |
| 00880304593008 | 16-104174 |
| 00880304592995 | 16-104172 |
| 00880304592988 | 16-104170 |
| 00880304592971 | 16-104168 |
| 00880304592964 | 16-104166 |
| 00880304592957 | 16-104164 |
| 00880304592940 | 16-104162 |
| 00880304592933 | 16-104160 |
| 00880304592926 | 16-104158 |
| 00880304592919 | 16-104156 |
| 00880304592902 | 16-104154 |
| 00880304592896 | 16-104152 |
| 00880304592889 | 16-104150 |
| 00880304592872 | 16-104148 |
| 00880304592865 | 16-104146 |
| 00880304592858 | 16-104144 |
| 00880304592841 | 16-104142 |
| 00880304592834 | 16-104140 |