| 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 |