Primary Device ID | 20185098000348 |
NIH Device Record Key | b9989d2d-676e-4bbb-8a40-650c8f2247b9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FlexPlus |
Version Model Number | ProM-039 |
Catalog Number | ProM-039 |
Company DUNS | 135741127 |
Company Name | PRO MEDICAL SUPPLIES, INC. |
Device Count | 800 |
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 | true |
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 | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com | |
Phone | 215-938-0200 |
sales@promedspecialties.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 18509800034480 [Unit of Use] |
GS1 | 20185098000348 [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 | 2016-07-26 |
00185098000757 | Electrodes Black Foam Back 1.75"x3.75" (1 pack = 4 electrodes per pack) |
00185098000177 | Electrodes Black Foam Back 2"Round (1 pack = 4 electrodes per pack) |
30185098000178 | Electrodes Black Foam Back 2" Round (400 packs per case - 4 electrodes per pack = 1600) |
20185098000751 | Electrodes Black Foam Back 1.75"x3.75" (200 packs per case - 4 electrodes per pack = 800) |
20185098000348 | Electrodes Black Foam (200 Pack Per Case -4 Electrodes Per Pack = 800) |
20185098000171 | Electrodes Black Foam Back 2" Round (100 packs per box - 4 electrodes per pack = 400) |
10185098000754 | Electrodes Black Foam 1.75"x3.75" (50 packs per case-4 electrodes per pack = 200) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLEXPLUS 78066463 2849137 Dead/Cancelled |
Dada Corporation 2001-05-30 |
FLEXPLUS 77728910 3770270 Live/Registered |
Pro Medical Supplies Inc. 2009-05-05 |
FLEXPLUS 77245563 3519053 Dead/Cancelled |
SPINEVISION, Société Anonyme 2007-08-02 |
FLEXPLUS 74624568 not registered Dead/Abandoned |
O.S.I. Corporation 1995-01-23 |
FLEXPLUS 74333511 1790045 Dead/Cancelled |
Virginia Abrasives Corporation 1992-11-23 |
FLEXPLUS 74270915 1805310 Live/Registered |
MARIETTA DRAPERY & WINDOW COVERINGS CO., INC. 1992-04-29 |
FLEXPLUS 73667985 1556767 Dead/Cancelled |
BLUE CROSS AND BLUE SHIELD OF GEORGIA, INC. 1987-06-18 |
FLEXPLUS 73643030 1475271 Dead/Cancelled |
NATIONAL ANNUITY PROGRAMS, INC. 1987-02-05 |