| Primary Device ID | 05415334002340 |
| NIH Device Record Key | 6933a9ba-3ff6-43d4-81ec-de67d13204c7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Coronis Fusion 4 MP |
| Version Model Number | MDCC-4430 |
| Company DUNS | 371618773 |
| Company Name | Barco NV |
| 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 | 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 | 05415334002340 [Primary] |
| PGY | Display, diagnostic radiology |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2019-10-15 |
| 05415334002340 | MDCC-4430 |
| 05415334028845 | MDCC-4430 MDT |
| 05415334025981 | MDCC-4430 NC |
| 05415334034785 | MDCC-4430 MDT MKII |