Primary Device ID | 00841517103392 |
NIH Device Record Key | 45fbd84a-4e6e-4cd2-a1ea-80bb4a5ffdda |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SonoSite X-Porte |
Version Model Number | P16055-70 |
Catalog Number | P16055 |
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 |
Storage Environment Humidity | Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841517103392 [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 | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-01-11 |
00841517104740 | P19220-22 |
00841517104733 | P19220-77 |
00841517104436 | P19220-75 |
00841517103415 | SonoSite X-Porte |
00841517103408 | P19220-20 |
00841517103392 | SonoSite X-Porte |
00841517103385 | SonoSite X-Porte |
00841517102821 | P17880-54 |
00841517102814 | P17880-11 |
00841517102807 | P17880-10 |
00841517102760 | P19220-55Â |
00841517102753 | P19220-10Â |
00841517102746 | P19220-05Â |
00841517102715 | P16055-60 |
00841517102708 | P16055-56 |
00841517102692 | P16055-35 |
00841517102685 | P16055-32 |
00841517101916 | P19220-65 |
00841517101909 | P19220-15 |
00841517100933 | P19220-60 |
00841517100926 | P17880-55 |
00841517104412 | P19220-21 |
00841517107420 | P20431-03 |