Protekt Titanium Adhesive Pre-Gelled Electrode for TENS - Round 2" PMTENSEL3

GUDID 05060488570971

Protekt Titanium Adhesive Pre-Gelled Electrode for TENS - Round 2"

PROACTIVE MEDICAL PRODUCTS, LLC

Transcutaneous electrical stimulation electrode
Primary Device ID05060488570971
NIH Device Record Key27113833-abcd-4052-9054-343a6efdc580
Commercial Distribution StatusIn Commercial Distribution
Brand NameProtekt Titanium Adhesive Pre-Gelled Electrode for TENS - Round 2"
Version Model NumberPMTENSEL3
Catalog NumberPMTENSEL3
Company DUNS078582655
Company NamePROACTIVE MEDICAL PRODUCTS, LLC
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 Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com
Phone+1 855 237 7622
Emailsales@proactivemedical.com

Device Dimensions

Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch
Height1 Inch
Width6 Inch
Length4 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS105060488570971 [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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-09
Device Publish Date2020-01-01

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