Primary Device ID | 00851920007026 |
NIH Device Record Key | fc024c6a-26ca-4f20-963e-babac8627b38 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ultraview DM3 |
Version Model Number | 91330-N |
Catalog Number | 175-6200 |
Company DUNS | 848429929 |
Company Name | ZOE MEDICAL INCORPORATED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851920007026 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-22 |
00851920007033 | The Ultraview DM3 Monitor is intended for monitoring, recording, and alarming basic vital signs |
00851920007026 | The Ultraview DM3 Monitor is intended for monitoring, recording, and alarming basic vital signs |
00851920007019 | The Ultraview DM3 Monitor is intended for monitoring, recording, and alarming basic vital signs |
00851920007002 | The Ultraview DM3 Monitor is intended for monitoring, recording, and alarming basic vital signs |