Gental Patch ProM-027

GUDID 20185098000812

(40) Electrodes 2.0"x2.0" Blue Gel Adhesive For Sensitive Skin (10 Packs per box = 4 Electrodes Per Pack)

PRO MEDICAL SUPPLIES, INC.

Transcutaneous electrical stimulation electrode
Primary Device ID20185098000812
NIH Device Record Key71949006-b7b1-493f-95e5-bd977fb324e7
Commercial Distribution StatusIn Commercial Distribution
Brand NameGental Patch
Version Model NumberProM-027
Catalog NumberProM-027
Company DUNS135741127
Company NamePRO MEDICAL SUPPLIES, INC.
Device Count40
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

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

Device Identifiers

Device Issuing AgencyDevice ID
GS118509800081840 [Unit of Use]
GS120185098000812 [Primary]

FDA Product Code

GXYElectrode, Cutaneous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-08-24

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