| Primary Device ID | 00841517104856 |
| NIH Device Record Key | 311ab8ef-80bd-4ee8-9d29-8faf4974ea4f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | L25x/13-6 MHz |
| Version Model Number | P22950-20 |
| Catalog Number | P22950 |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *N/A |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841517104856 [Primary] |
| IYN | System, imaging, pulsed doppler, ultrasonic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-08-01 |
| Device Publish Date | 2019-07-24 |
| 00841517105006 | Diagnostic Ultrasound Transducer |
| 00841517104863 | Diagnostic Ultrasound Transducer |
| 00841517104856 | Diagnostic Ultrasound Transducer |
| 00841517102906 | Diagnostic Ultrasound Transducer |
| 00841517102258 | Diagnostic Ultrasound Transducer |
| 00841517102241 | Diagnostic Ultrasound Transducer |
| 00841517100445 | Diagnostic Ultrasound Transducer |
| 00841517100438 | Diagnostic Ultrasound Transducer |
| 00841517106942 | Diagnostic Ultrasound Transducer |
| 00841517107581 | P22950-20A |
| 00841517107932 | Diagnostic Ultrasound Transducer |
| 00841517109110 | Diagnostic Ultrasound Transducer |
| 00841517108946 | Diagnostic Ultrasound Transducer |