Primary Device ID | 06942820461767 |
NIH Device Record Key | e01174f2-6527-4768-befd-b0744c72963e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Virtuox |
Version Model Number | VPOD Freedom |
Company DUNS | 526882823 |
Company Name | Beijing Choice Electronic Technology Co., Ltd. |
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 | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06942820461767 [Primary] |
DQA | Oximeter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2018-01-12 |
06942820461767 | Wrist Pulse Oximeter |
06942820462115 | VIRTUOX Vital Sign Monitor VPOD VITAL PRO |
06942820462108 | VIRTUOX Pulse Oximeter VPOD H PRO |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VIRTUOX 87555085 5588807 Live/Registered |
VirtuOx, Inc. 2017-08-03 |
VIRTUOX 78858171 3211053 Dead/Cancelled |
Virtuox, Inc. 2006-04-10 |