| Primary Device ID | 00841517104672 |
| NIH Device Record Key | 55cfeea7-5bf8-4ed0-b13b-b0d046201a2a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UHF22 Transducer |
| Version Model Number | 51414-50A |
| Catalog Number | 51414 |
| 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 |
| xx@xx.xx |
| Handling Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841517104672 [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 | 2019-03-21 |
| Device Publish Date | 2019-03-13 |
| 00841517104672 | Diagnostic Ultrasound Transducer |
| 00841517104511 | Diagnostic Ultrasound Transducer |
| 00841517102319 | Diagnostic Ultrasound Transducer |
| 00841517102302 | Diagnostic Ultrasound Transducer |
| 00841517100704 | Diagnostic Ultrasound Transducer |
| 00841517100698 | Diagnostic Ultrasound Transducer |