Primary Device ID | 00841517102067 |
NIH Device Record Key | ef05feb4-f3e4-4491-9af0-c66247e75f1d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | H-Universal Stand |
Version Model Number | P12163-16 |
Catalog Number | P12163 |
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 |
Handling Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841517102067 [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 | 2017-03-31 |
00841517102173 | Diagnostic Ultrasound System Accessory |
00841517102135 | Diagnostic Ultrasound System Accessory |
00841517102067 | Diagnostic Ultrasound System Accessory |
00841517101756 | Diagnostic Ultrasound System Accessory |
00841517100070 | Diagnostic Ultrasound System Accessory |
00841517105761 | Diagnostic Ultrasound System Accessory |
00841517106430 | Diagnostic Ultrasound System Accessory |
00841517108120 | Diagnostic Ultrasound System Accessory |