Marc Pro, Inc

GUDID 00854784005023

Electrode, Cutaneous

MARC PRO

Transcutaneous electrical stimulation electrode
Primary Device ID00854784005023
NIH Device Record Key747aa021-21eb-41f3-850e-5347d15e15c2
Commercial Distribution StatusIn Commercial Distribution
Brand NameMarc Pro, Inc
Version Model Number70011
Company DUNS042947847
Company NameMARC PRO
Device Count1
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 Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com
Phone855-627-2776
Emailcontact@marcpro.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100854784005023 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GXYElectrode, Cutaneous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-15

On-Brand Devices [Marc Pro, Inc]

00854784005023Electrode, Cutaneous
00854784005016MPP

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