| Primary Device ID | 00884838103641 | 
| NIH Device Record Key | 38575938-2391-4c8a-a240-06da527a2ca8 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | XS-100 X-Ray Tube Assembly | 
| Version Model Number | 3000-048-52391 | 
| Catalog Number | 3000-048-52391 | 
| 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 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00884838103641 [Primary] | 
| ITY | Assembly, tube housing, x-ray, diagnostic | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2020-12-10 | 
| Device Publish Date | 2020-12-02 | 
| 00884838083455 | diagnostic x-ray tube housing assembly | 
| 00884838070868 | diagnostic x-ray tube housing assembly | 
| 00884838103641 | diagnostic x-ray tube housing assembly | 
| 00884838103634 | diagnostic x-ray tube housing assembly | 
| 00884838108158 | diagnostic x-ray tube housing assembly | 
| 00884838107243 | diagnostic x-ray tube housing assembly | 
| 00884838113749 | Diagnostic x-ray tube housing assembly |