| Primary Device ID | 00841517102791 |
| NIH Device Record Key | 3f930a43-3696-43b1-a2ad-d54589296712 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Edge Stand |
| Version Model Number | P15800-25 |
| Catalog Number | P15800 |
| 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 Humidity | Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841517102791 [Primary] |
| IYN | System, imaging, pulsed doppler, 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 | 2017-09-22 |
| 00841517102791 | P15800-25 |
| 00841517102784 | P15800-21 |
| 00841517102777 | P15800-16 |
| 00841517102142 | Diagnostic Ultrasound System Accessory |
| 00841517102074 | P15800-27 |
| 00841517100025 | Diagnostic Ultrasound System Accessory |
| 00841517105785 | P15800-50 |
| 00841517106447 | Diagnostic Ultrasound System Accessory |
| 00841517108137 | Ultrasound Accessory |