| Primary Device ID | 00841517104313 |
| NIH Device Record Key | 12a8eb7d-a84f-4b70-9d4c-d22af48c01cb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SonoSite iViz |
| Version Model Number | P20830-52 |
| Catalog Number | P20830 |
| 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 |
| Storage Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841517104313 [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 | 2020-06-30 |
| Device Publish Date | 2020-06-22 |
| 00841517104566 | Diagnostic ultrasound system |
| 00841517103842 | Diagnostic ultrasound system |
| 00841517103835 | Diagnostic ultrasound system |
| 00841517103712 | Diagnostic ultrasound system |
| 00841517102203 | Diagnostic ultrasound system |
| 00841517101862 | Diagnostic ultrasound system |
| 00841517101855 | Diagnostic ultrasound system |
| 00841517101671 | Diagnostic ultrasound system |
| 00841517101572 | Diagnostic ultrasound system |
| 00841517101442 | Diagnostic ultrasound system |
| 00841517101206 | Diagnostic ultrasound system |
| 00841517100896 | Diagnostic ultrasound system |
| 00841517104719 | P20830-26 |
| 00841517104313 | Diagnostic ultrasound system |
| 00841517107468 | 1 |