| Primary Device ID | 00884838097872 |
| NIH Device Record Key | 30f806d3-7114-413d-801b-523ed3a5b4d6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EPIQ 7C ULTRASOUND SYSTEM |
| Version Model Number | 795201 |
| Company DUNS | 063377717 |
| Company Name | Philips Ultrasound, Inc. |
| 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 | 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 | 00884838097872 [Primary] |
| ITX | Transducer, ultrasonic, 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 | 2020-08-24 |
| Device Publish Date | 2020-08-14 |
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| 00884838123977 - EPIQ CVxi Diagnostic Ultrasound System | 2024-06-06 VM 11.0 Update |
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| 00884838114265 - Affinti 30 Diagnostic Ultrasound System Circular Edition | 2024-06-04 VM10.0 Update |
| 00884838114241 - Affinti 50 Diaagnostic Ultrasound System Circular Edition | 2024-05-13 Software Version 10.0.2 |
| 00884838114258 - Affinti 70 Diaagnostic Ultrasound System Circular Edition | 2024-05-13 Software Version 10.0.2 |
| 00884838114203 - EPIQ 7 Diagnostic Ultrasound System Circular Edition | 2024-04-18 10.0.X Circular Edition |