Flex Plus ProM-039
GUDID 10185098000341
Electrodes Black Foam (50 Pack Per Box -4 Electrodes Per Pack = 200)
PRO MEDICAL SUPPLIES, INC.
Transcutaneous electrical stimulation electrode, single-use| Primary Device ID | 10185098000341 |
| NIH Device Record Key | 2a3b5498-0aa2-4ded-ae10-34b3e6b859c2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Flex Plus |
| Version Model Number | ProM-039 |
| Catalog Number | ProM-039 |
| Company DUNS | 135741127 |
| Company Name | PRO MEDICAL SUPPLIES, INC. |
| Device Count | 200 |
| 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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10185098000341 [Primary] |
| GS1 | 18509800034420 [Unit of Use] |
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 | 4 |
| Public Version Date | 2021-02-19 |
| Device Publish Date | 2016-07-26 |
On-Brand Devices [Flex Plus]
| 00185098000344 | Electrodes Black 2.0"x4.0" (1 Pack = 4 Electrodes Per Pack) |
| 00185098000108 | Electrodes - Flex Plus -2.0" x 2.0" (1 pack = 4 electrodes per pack) |
| 30185098000109 | Electrodes Flex Plus 2.0"x2.0" (400 packs per case - 4 electrodes per pack = 1600 pieces) |
| 20185098000102 | Electrodes Flex Plus 2.0" x 2.0" (100 pack per box - 4 electrodes per pack = 400 pieces) |
| 10185098000341 | Electrodes Black Foam (50 Pack Per Box -4 Electrodes Per Pack = 200) |
Trademark Results [Flex Plus]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FLEX PLUS 90463013 not registered Live/Pending |
Smart Flex, Inc 2021-01-13 |
 FLEX PLUS 78357612 not registered Dead/Abandoned |
W.F. YOUNG, INCORPORATED 2004-01-26 |
 FLEX PLUS 76413264 not registered Dead/Abandoned |
Anthony R. Scheiber, D.V.M., P.C. 2002-05-23 |
 FLEX PLUS 74160120 1678704 Dead/Cancelled |
Proform Fitness Products, Inc. 1991-04-23 |
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