| Primary Device ID | 04048844146375 |
| NIH Device Record Key | 3fb40e3d-9ae5-4dee-8601-3d12a106c557 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MUTARS® trial connecting part proximal |
| Version Model Number | 7730010002 |
| Company DUNS | 324369826 |
| Company Name | implantcast GmbH |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04048844146375 [Primary] |
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04048844146375]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-09 |
| Device Publish Date | 2019-04-01 |
| 04048844358617 - MUTARS® | 2026-04-01 intramedullary drill |
| 04048844358716 - MUTARS® | 2026-04-01 intramedullary drill |
| 04048844358792 - MUTARS® | 2026-04-01 intramedullary drill |
| 04048844358839 - MUTARS® | 2026-04-01 intramedullary drill |
| 04048844732103 - n/a | 2026-04-01 resection guide |
| 04048844738150 - implaFit® | 2026-04-01 broach handle straight |
| 04048844731977 - implaFit® | 2026-03-30 short stem broach |
| 04048844731984 - implaFit® | 2026-03-30 short stem broach |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MUTARS 79189818 5135143 Live/Registered |
implantcast GmbH 2016-05-17 |