| Primary Device ID | 04046768148321 |
| NIH Device Record Key | 938cc9b5-49dc-46fa-be51-f93dce6f9816 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Retrofit kit head fixation I |
| Version Model Number | 116036A0 |
| Company DUNS | 315435859 |
| Company Name | MAQUET GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 | 04046768148321 [Primary] |
| BWN | Table And Attachments, Operating-Room |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-29 |
| Device Publish Date | 2024-11-21 |
| 04046768148321 - Retrofit kit head fixation I | 2024-11-29 |
| 04046768148321 - Retrofit kit head fixation I | 2024-11-29 |
| 04046768148338 - Extension plate | 2024-11-29 |
| 04046768148345 - Extension plate | 2024-11-29 |
| 04046768148352 - Extension plate | 2024-11-29 |
| 04046768150973 - Extension plate | 2024-11-29 |
| 04046768151208 - Retrofit kit head fixation II | 2024-11-29 |
| 04046768145993 - Universal Remote Control | 2024-09-26 |
| 04046768148475 - Table width extension, long | 2024-06-11 |