Primary Device ID | 00841517104481 |
NIH Device Record Key | 2c010e09-cf30-4067-ae86-f01c5d9678fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SonoSite SII |
Version Model Number | P23620-17 |
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 |
Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841517104481 [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 | 2 |
Public Version Date | 2020-03-02 |
Device Publish Date | 2019-01-11 |
00841517105549 | Diagnostic ultrasound system |
00841517105532 | Diagnostic ultrasound system |
00841517105525 | Diagnostic ultrasound system |
00841517105303 | Diagnostic ultrasound system |
00841517104702 | Diagnostic ultrasound system |
00841517104580 | Diagnostic ultrasound system |
00841517104573 | Diagnostic Ultrasound System |
00841517104481 | Diagnostic ultrasound system |
00841517104474 | Diagnostic ultrasound system |
00841517104467 | Diagnostic ultrasound system |
00841517103774 | SONOSITE SII ULTRASOUND SYSTEM, DTC, 1.2.1, REMANUFACTURED, ROHS |
00841517103767 | SONOSITE SII ULTRASOUND SYSTEM, STC, 1.2.1, REMANUFACTURED, ROHS |
00841517103682 | Diagnostic ultrasound system |
00841517103675 | Diagnostic ultrasound system |
00841517103613 | P23630-14 |
00841517103606 | P23620-14 |
00841517103583 | P20883-14 |
00841517103569 | P20500-14 |
00841517102470 | P23630-13 |
00841517102463 | P23620-13 |
00841517102456 | P23630-13R |
00841517102449 | P23620-13R |
00841517102425 | P20883-13R |
00841517102401 | Diagnostic ultrasound system |
00841517102012 | P20883-13 |
00841517101985 | P20500-13 |
00841517101824 | P23620-10 |
00841517101800 | Diagnostic ultrasound system |
00841517101411 | P20883-12 |
00841517101398 | P20500-12 |
00841517101251 | P20883-10 |
00841517100216 | P20500-10 |
00841517106751 | P24550-41R |
00841517106744 | P24550-41 |
00841517107475 | 1 |
00841517107918 | SYSTEM JANUS E 4.0 |
00841517109202 | P24550-45 |
00841517109172 | P23620-45 |
00841517109691 | Diagnostic Ultrasound Device |
00841517109783 | Diagnostic ultrasound device |
00841517110154 | Diagnostic ultrasound system |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SONOSITE SII 86687120 5032988 Live/Registered |
FUJIFILM SonoSite, Inc. 2015-07-08 |