| Primary Device ID | 00884838103221 |
| NIH Device Record Key | 84a016c4-49c8-4a37-8ae5-0a6a042de282 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProxiDiagnost N90 |
| Version Model Number | 706110 |
| Company DUNS | 314101218 |
| Company Name | Philips Medical Systems DMC GmbH |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| 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 | 00884838103221 [Primary] |
| JAA | System, X-Ray, Fluoroscopic, Image-Intensified |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-01-25 |
| Device Publish Date | 2022-01-17 |
| 00884838097315 - Anti-scatter Grid (60/10/180) | 2024-01-26 |
| 00884838097322 - Anti-scatter Grid (60/10/140) | 2024-01-26 |
| 00884838097339 - Anti-scatter Grid (60/10/110) | 2024-01-26 |
| 00884838105454 - CT4000 | 2023-09-08 diagnostic x-ray tube housing assembly |
| 00884838113749 - XS-100 X-Ray Tube Assembly | 2023-09-08 Diagnostic x-ray tube housing assembly |
| 00884838121379 - CT3000 | 2023-09-08 Diagnostic x-ray tube housing assembly |
| 00884838121386 - CT4000 | 2023-09-08 Diagnostic x-ray tube housing assembly |
| 00884838097506 - Anti-scatter Grid (36/12/100) | 2023-08-14 |