| Primary Device ID | 00841517103071 |
| NIH Device Record Key | 865e3599-255c-496f-880b-44b11a31c6b9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SonoSite S-Series |
| Version Model Number | P09417-65R |
| Catalog Number | P09417 |
| 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(999)999-9999 |
| xyz@xyz.com |
| Handling Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841517103071 [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 | 2017-10-24 |
| 00841517105495 | P09417-71R |
| 00841517105488 | P09417-95R |
| 00841517103101 | P09417-68R |
| 00841517103095 | P09417-67R |
| 00841517103088 | P09417-66R |
| 00841517103071 | P09417-65R |
| 00841517103064 | P09417-57R |
| 00841517102623 | P09417-92 |
| 00841517102616 | P09417-68 |
| 00841517101794 | P09417-94R |
| 00841517101787 | P09417-70R |
| 00841517101701 | P09417-94 |
| 00841517101695 | SONOSITE S SERIES ULTRASOUND SYSTEM, S1.9.2 |
| 00841517101312 | P09417-69R |
| 00841517101305 | P09417-69 |
| 00841517100285 | P09417-93R |
| 00841517100278 | P09417-93 |
| 00841517105730 | P28962-95 |
| 00841517105716 | P28962-95R |