| Primary Device ID | 00884838129771 |
| NIH Device Record Key | 7f046419-91c1-407c-a456-c3328ddeaaa8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LVivo View Selection |
| Version Model Number | 3.1.0.0 |
| Company DUNS | 063377717 |
| Company Name | Philips Ultrasound LLC |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | 00884838129771 [Primary] |
| QIH | Automated Radiological Image Processing Software |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-26 |
| Device Publish Date | 2025-12-18 |
| 00884838129771 - LVivo View Selection | 2025-12-26 |
| 00884838129771 - LVivo View Selection | 2025-12-26 |
| 00884838130913 - Lumify Diagnostic Ultrasound System | 2025-12-24 Lumify Rugged System Bundle |
| 00884838129276 - Ultrasound Workspace | 2025-09-08 Device Model: 300013759461 |
| 00884838123625 - Ultrasound System 5500CV | 2025-07-28 As part of SW 2.0 |
| 00884838123632 - Ultrasound System 5500P | 2025-07-28 Part of SW 2.0 |
| 00884838123649 - Ultrasound System 5500W | 2025-07-28 Part of SW 2.0 |
| 00884838123656 - Ultrasound System 5300G | 2025-07-28 Part of SW 2.0 |
| 00884838123663 - Ultrasound System 5300W | 2025-07-28 As part of SW 2.0 |