FlexPlus ProM-029
GUDID 30185098000178
Electrodes Black Foam Back 2" Round (400 packs per case - 4 electrodes per pack = 1600)
PRO MEDICAL SUPPLIES, INC.
Transcutaneous electrical stimulation electrode| Primary Device ID | 30185098000178 |
| NIH Device Record Key | acfc90f0-9370-419b-a6c5-c78cf9a99267 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FlexPlus |
| Version Model Number | ProM-029 |
| Catalog Number | ProM-029 |
| Company DUNS | 135741127 |
| Company Name | PRO MEDICAL SUPPLIES, INC. |
| Device Count | 1600 |
| 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 |
Customer Support Contacts
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 18509800017716 [Unit of Use] |
| GS1 | 30185098000178 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K132998
FDA Product Code
| GXY | Electrode, Cutaneous |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-07-26 |
On-Brand Devices [FlexPlus]
| 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) |
Trademark Results [FlexPlus]
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.