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 |
00841517110451 | Diagnostic Ultrasound Transducer |
00841517110499 | Diagnostic Ultrasound Transducer |