FDA UDI In Commercial Distribution 🇺🇸 United States

Liberty Multi-Mode Stimulator

DI: 00860000178303 · Model: LMS 1000 · LIBERTY MEDICAL SOLUTIONS, LLC
Product Codes
3
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Liberty Multi-Mode Stimulator
Primary DI
00860000178303
Version / Model
LMS 1000
Company Name
LIBERTY MEDICAL SOLUTIONS, LLC
Labeler DUNS
055350856
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-17
Public Version
6
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
b34acc71-3c9d-436a-bf99-3340a95e6a91

Device Description

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.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
IPF Stimulator, Muscle, Powered
LIH Interferential Current Therapy

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system
35372 Analgesic transcutaneous electrical nerve stimulation system
36737 Interferential electrical stimulation system

Identifiers

Type ID
Primary 00860000178303

Customer Contacts

Phone
8009320147

Premarket Submissions

Submission Number Supplement Number
K093138 000