Liberty Multi-Mode Stimulator

GUDID 00860000178303

The Liberty Medical Solutions, LLC Multi-Mode Stimulator (MMS) (the Device) is a battery powered electrotherapy device intended for clinic and outpatient rehabilitative therapy, acute postoperative care and home use for patients suffering from a variety of chronic pain issues. Prescribed by a physician, it gives the clinician a variety of electrotherapy modes to treat a range of indications. The MMS is designed for clinician and patient ease of use and provides safe and effective dispensing of the desired electrotherapy treatment. The Intended Use Environment is Home Healthcare but the Device can also be used in a Chiropractic, Physical Therapy or Pain Management Clinic. The Device uses a tactile button user interface for control of the operating system and therapy amplitude settings. The Device has a liquid crystal character display which provides information to the user and displays the current therapy settings. The Device’s therapeutic output is transmitted through the patient lead wires to the cutaneous hydrogel electrodes affixed to the user’s skin. The energy generated by the Device is conveyed, via the patient lead wires and cutaneous electrodes, through the patients skin to excite either the underlying motor nerves to elicit involuntary muscle contractions or the sensory nerves to manage pain.

LIBERTY MEDICAL SOLUTIONS, LLC

Physical therapy transcutaneous neuromuscular electrical stimulation system
Primary Device ID00860000178303
NIH Device Record Keyb34acc71-3c9d-436a-bf99-3340a95e6a91
Commercial Distribution StatusIn Commercial Distribution
Brand NameLiberty Multi-Mode Stimulator
Version Model NumberLMS 1000
Company DUNS055350856
Company NameLIBERTY MEDICAL SOLUTIONS, 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 Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com
Phone8009320147
Emailinfo@lmstens.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860000178303 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GZJStimulator, Nerve, Transcutaneous, For Pain Relief

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-23
Device Publish Date2018-08-17
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