ProM-500 ProM-500

GUDID 10185098000051

(30) Per Case -Electric Muscle Stimulator -Three Mode Dual Channel 4 Leads -Zipper Case Includes, device, lead wires, 9V battery and (1) pack of electrodes, dual language instruction manual

PRO MEDICAL SUPPLIES, INC.

Transcutaneous electrical stimulation electrode, single-use
Primary Device ID10185098000051
NIH Device Record Keyf8611f2e-7fa7-4e9b-b2c0-8707188e14a1
Commercial Distribution StatusIn Commercial Distribution
Brand NameProM-500
Version Model NumberProM-500
Catalog NumberProM-500
Company DUNS135741127
Company NamePRO MEDICAL SUPPLIES, INC.
Device Count30
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com
Phone215-938-0200
Emailsales@promedspecialties.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110185098000051 [Primary]
GS118509800005430 [Unit of Use]

FDA Product Code

IPFStimulator, Muscle, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-02-19
Device Publish Date2016-08-24

On-Brand Devices [ProM-500]

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

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