| Primary Device ID | 00884838092907 |
| NIH Device Record Key | 35dc2d93-32f5-4a07-9c40-b13585dcc1f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DA200ULTRA |
| Version Model Number | 9896-055-88704 |
| Catalog Number | 9896-055-88704 |
| Company DUNS | 314101218 |
| Company Name | Philips Medical Systems DMC GmbH |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 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 |