| Primary Device ID | 00853177007101 | 
| NIH Device Record Key | dffbc850-466b-4af9-bbc2-53e17ebb1cc4 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Mediflex | 
| Version Model Number | 710582-003 | 
| 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 | 00853177007101 [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 |