Mobius Therapy

GUDID 00860074002207

Endless Relief

Analgesic transcutaneous electrical nerve stimulation system
Primary Device ID00860074002207
NIH Device Record Keyaeaf601d-d48e-40aa-9838-ed95fcd2056c
Commercial Distribution Discontinuation2023-05-31
Commercial Distribution StatusIn Commercial Distribution
Brand NameMobius Therapy
Version Model NumberKTR-201
Company DUNS081154948
Company NameEndless Relief
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com
Phone303-601-4009
Emailfhorwich@endlessrelief.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860074002207 [Primary]
GS100860074002238 [Package]
Package: Carton [40 Units]
Discontinued: 2023-05-31
In Commercial Distribution

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 Number2
Public Version Date2019-10-23
Device Publish Date2018-06-30

On-Brand Devices [Mobius Therapy]

00860074002245PAD2
00860074002207KTR-201

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