| Primary Device ID | 00884838076099 |
| NIH Device Record Key | 9e5d0071-266b-4e5a-bc98-550a3770d697 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SRM 2250 ROT-GS 504 |
| Version Model Number | 9890-000-63842 |
| Catalog Number | 9890-000-63842 |
| 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 |