| Primary Device ID | 00185098000030 |
| NIH Device Record Key | a67c723b-97ec-49cc-b717-a8b6d3ac6246 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProM-300 |
| Version Model Number | ProM-300 |
| Catalog Number | ProM-300 |
| Company DUNS | 135741127 |
| Company Name | PRO MEDICAL SUPPLIES, INC. |
| 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 | false |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| 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 | 00185098000030 [Primary] |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-08-24 |
| 00185098000030 | (1) -Transcutaneous Nerve Stimulator -Three Mode with Timer Dual Channel 4 Leads - Zipper Case I |
| 10185098000037 | (30) Per Case -Transcutaneous Nerve Stimulator -Three Mode with Timer Dual Channel 4 Leads - Zi |