| Primary Device ID | 08033390066532 |
| NIH Device Record Key | af5e5048-b577-45bd-8237-47f454f0fb36 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | C2 Hip |
| Version Model Number | 9045.12.020 |
| Catalog Number | 9045.12.020 |
| Company DUNS | 432066322 |
| Company Name | LIMACORPORATE SPA |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| 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 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08033390066532 [Primary] |
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08033390066532]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-07-05 |
| Device Publish Date | 2018-03-13 |
| 08033390071673 | M8 Stem Beater-Extractor |
| 08033390071666 | C2 Hip - Lateralized Trial Neck |
| 08033390071659 | C2 Hip - Trial Neck |
| 08033390066594 | C2 Hip - Broach # 6 |
| 08033390066556 | C2 Hip - Broach # 2 |
| 08033390066549 | C2 Hip - Broach # 1 |
| 08033390066532 | C2 Hip - Broach # 0 |
| 08033390066525 | C2 Hip - Broach # 01 |
| 08033390066655 | C2 Hip - Broach # 12 |
| 08033390066648 | C2 Hip - Broach # 11 |
| 08033390066631 | C2 Hip - Broach # 10 |
| 08033390066624 | C2 Hip - Broach # 9 |