| Primary Device ID | 00841517100759 |
| NIH Device Record Key | 3e0a1cbd-7243-42e0-bd50-fca3c323be29 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vevo MD Imaging System |
| Version Model Number | 51475-10 |
| Catalog Number | 51475 |
| Company DUNS | 014438860 |
| Company Name | FUJIFILM SONOSITE, 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 | false |
| Serial Number | true |
| 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 |
| Phone | 1-877-657-8118 |
| ffss-service@fujifilm.com |
| Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841517100759 [Primary] |
| IYO | System, imaging, pulsed echo, ultrasonic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-21 |
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| 00841517102548 | Diagnostic ultrasound system |
| 00841517102524 | Diagnostic ultrasound system |
| 00841517100766 | Diagnostic ultrasound system |
| 00841517100759 | Diagnostic ultrasound system |
| 00841517109790 | Diagnostic ultrasound system |
| 00841517110123 | Diagnostic ultrasound system |