Primary Device ID | 00817613020482 |
NIH Device Record Key | 003f8b5e-12bf-45a3-a2d2-922121ed3b72 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Winmate |
Version Model Number | W1500 |
Catalog Number | W1500 |
Company DUNS | 051244569 |
Company Name | MED X CHANGE, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817613020482 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-11-05 |
Device Publish Date | 2018-10-05 |
00817613020482 | 15.6” Multi-Touch Chassis Display Projective-Capacitive Touch Monitor |
00817613020475 | Winmate 15.6” Multi-Touch Chassis Display Projective-Capacitive Touch Monitor |
00817613021311 | W1500M Winmate Display |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() WINMATE 90354568 not registered Live/Pending |
Willinox Trading Company Limited 2020-12-02 |
![]() WINMATE 87550067 5426849 Live/Registered |
WINMATE INC. 2017-07-31 |
![]() WINMATE 78930300 3356322 Dead/Cancelled |
WINMATE INC. 2006-07-15 |
![]() WINMATE 74291989 1842714 Dead/Cancelled |
Tandy Corporation 1992-07-06 |
![]() WINMATE 73441592 1328593 Dead/Cancelled |
Crompton Company, Inc. 1983-08-29 |