| Primary Device ID | 00884838070851 | 
| NIH Device Record Key | 173f8990-428a-4059-9266-93a74419b6b0 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | XS-100 Generator | 
| Version Model Number | 9806-058-00221 | 
| Catalog Number | 9806-058-00221 | 
| 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 |