| Primary Device ID | 05415334046177 |
| NIH Device Record Key | 445e25f4-3632-4f06-8876-52962ff9faf7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Eonis 24” |
| Version Model Number | MDRC-2424 |
| Catalog Number | K9356051A1X |
| Company DUNS | 371618773 |
| Company Name | Barco NV |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05415334046177 [Primary] |
| LMD | System, Digital Image Communications, Radiological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-21 |
| Device Publish Date | 2023-12-13 |
| 05415334046191 | MDRC-2424 HPEW |
| 05415334046184 | MDRC-2424 HTIB |
| 05415334046177 | MDRC-2424 HNEW |
| 05415334046160 | MDRC-2424 STIB |
| 05415334046153 | MDRC-2424 HNIB |
| 05415334046030 | MDRC-2424 SNIB |
| 05415334046023 | MDRC-2424 HTEW |