PROBE W/GERMANIUM DIODE

GUDID 14897076720689

TENS PLUS INDUSTRIAL COMPANY

Transcutaneous electrical stimulation lead
Primary Device ID14897076720689
NIH Device Record Key3a71dee9-dadf-4e72-bb54-aa349ca96770
Commercial Distribution StatusIn Commercial Distribution
Brand NamePROBE W/GERMANIUM DIODE
Version Model NumberIon.ES.Abso
Company DUNS663211978
Company NameTENS PLUS INDUSTRIAL COMPANY
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS114897076720689 [Primary]

FDA Product Code

KNMDevice, Pressure Applying

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-22
Device Publish Date2022-11-14

Devices Manufactured by TENS PLUS INDUSTRIAL COMPANY

14897076721457 - Lion.Warm.XL2023-06-13
14897076721655 - Multi.D.1.52023-06-13
14897076721815 - Moxa.Bx.BamS2023-06-13
14897076721822 - Moxa.Bx.BamL2023-06-13
14897076721853 - Pistol2023-06-13
14897076721860 - Pistol.Long2023-06-13
14897076721877 - Ins.MP.S2023-06-13
14897076721884 - Ins.MP.M2023-06-13

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