Primary Device ID | 00853177007156 |
NIH Device Record Key | f8e2ea32-a142-43e9-822d-710410aa09fa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mediflex |
Version Model Number | 710598-004 |
Company DUNS | 832979079 |
Company Name | TRUMEDICAL SOLUTIONS, LLC |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com | |
Phone | 423-910-0100 |
customerservice@tru-medical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00853177007156 [Primary] |
GXY | Electrode, Cutaneous |
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 | 2016-10-25 |
00853177007156 | Mediflex™ Foam-Backed Reusable Electrode, 2" x 3.5" Rectangle 4/Pkg. |
00853177007149 | Mediflex™ Foam-Backed Reusable Electrode, 2.75" Round 4/Pkg. |
00853177007132 | Mediflex™ Foam-Backed Reusable Electrode, 2" x 2" Square 4/Pkg. |
00853177007125 | Mediflex™ Foam-Backed Reusable Electrode, 2" Round 4/Pkg. |
00853177007118 | Mediflex™ Cloth-Backed Reusable Electrode, 2" x 3.5" Rectangle 4/Pkg. |
00853177007101 | Mediflex™ Cloth-Backed Reusable Electrode, 2.75" Round 4/Pkg. |
00853177007095 | Mediflex™ Cloth-Backed Reusable Electrode, 2" x 2" Square 4/Pkg. |
00853177007088 | Mediflex™ Cloth-Backed Reusable Electrode, 2" Round 4/Pkg. |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEDIFLEX 87338629 not registered Dead/Abandoned |
Lück GmbH & Co. KG 2017-02-16 |
MEDIFLEX 86572338 5306955 Live/Registered |
Matthew DeBow 2015-03-23 |
MEDIFLEX 86356077 4820817 Live/Registered |
Flexbar Machine Corp. 2014-08-04 |
MEDIFLEX 85874011 not registered Dead/Abandoned |
Lück GmbH & Co. KG 2013-03-12 |
MEDIFLEX 85274993 not registered Dead/Abandoned |
Weidlinger Associates, Inc. 2011-03-23 |
MEDIFLEX 79072519 3927818 Dead/Cancelled |
docPrice GmbH 2009-06-23 |
MEDIFLEX 78560178 not registered Dead/Abandoned |
Jordan Drew Corporation 2005-02-03 |
MEDIFLEX 77928929 3959077 Dead/Cancelled |
Jordan Drew Corporation 2010-02-05 |
MEDIFLEX 75086394 2186327 Live/Registered |
MYLAN TECHNOLOGIES, INC. 1996-04-10 |
MEDIFLEX 74553547 2055794 Dead/Cancelled |
Ehrenfried, Ted R. 1994-07-25 |
MEDIFLEX 74397558 1856677 Live/Registered |
FLEXBAR MACHINE CORP. 1993-06-04 |
MEDIFLEX 74293544 1794205 Dead/Cancelled |
COOPERVISION, INC. 1992-07-10 |