Low-Frequency Therapy Instrument

GUDID 06924607700696

Shenzhen Kentro Medical Electronics Co.,Ltd

Analgesic transcutaneous electrical nerve stimulation system
Primary Device ID06924607700696
NIH Device Record Key433a7a2b-fbf5-49ae-b32e-59e2fd06b362
Commercial Distribution StatusIn Commercial Distribution
Brand NameLow-Frequency Therapy Instrument
Version Model NumberKTR-206
Company DUNS544395368
Company NameShenzhen Kentro Medical Electronics Co.,Ltd
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

Device Identifiers

Device Issuing AgencyDevice ID
GS106924607700696 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NUHStimulator, Nerve, Transcutaneous, Over-The-Counter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-10-23
Device Publish Date2017-09-11

On-Brand Devices [Low-Frequency Therapy Instrument]

06924607700696KTR-206
06924607700603KTR-203
06924607700580KTR-202
06924607700535KTR-201

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