| Primary Device ID | 04048844105013 |
| NIH Device Record Key | 66464366-1972-486f-8815-f56409d1e601 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | cancellous screw angle stable |
| Version Model Number | 57944232 |
| Company DUNS | 324369826 |
| Company Name | implantcast GmbH |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 04048844105013 [Primary] |
| HSD | Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-02-19 |
| Device Publish Date | 2020-11-18 |
| 04048844105051 | 57944240 |
| 04048844105044 | 57944238 |
| 04048844105037 | 57944236 |
| 04048844105020 | 57944234 |
| 04048844105013 | 57944232 |
| 04048844105006 | 57944230 |
| 04048844104993 | 57944228 |
| 04048844104986 | 57944226 |
| 04048844104979 | 57944224 |
| 04048844104962 | 57944222 |
| 04048844104955 | 57944220 |
| 04048844104948 | 57944218 |
| 04048844104931 | 57944216 |
| 04048844104924 | 57944214 |
| 04048844104917 | 57944212 |
| 04048844104900 | 57944210 |