Primary Device ID | 10185098000051 |
NIH Device Record Key | f8611f2e-7fa7-4e9b-b2c0-8707188e14a1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProM-500 |
Version Model Number | ProM-500 |
Catalog Number | ProM-500 |
Company DUNS | 135741127 |
Company Name | PRO MEDICAL SUPPLIES, INC. |
Device Count | 30 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10185098000051 [Primary] |
GS1 | 18509800005430 [Unit of Use] |
IPF | Stimulator, Muscle, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2021-02-19 |
Device Publish Date | 2016-08-24 |
00185098000054 | (1) -Electric Muscle Stimulator -Three Mode Dual Channel 4 Leads -Zipper Case Includes, device, |
10185098000051 | (30) Per Case -Electric Muscle Stimulator -Three Mode Dual Channel 4 Leads -Zipper Case Includes |