| Primary Device ID | 07613327032895 |
| NIH Device Record Key | e2c4459c-096b-44c2-bc44-acc5fcecde6b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LFIT |
| Version Model Number | 6260-8-336 |
| Catalog Number | 6260-8-336 |
| Company DUNS | 058311945 |
| Company Name | Howmedica Osteonics Corp. |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Outer Diameter | 36 Millimeter |
| Outer Diameter | 36 Millimeter |
| Outer Diameter | 36 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327032895 [Primary] |
| 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 | 4 |
| Public Version Date | 2020-04-06 |
| Device Publish Date | 2015-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LFIT 86856174 not registered Dead/Abandoned |
Lblauas Group Holdings LLC 2015-12-21 |