FDA UDI In Commercial Distribution 🇺🇸 United States

NeuroMove

DI: 00852670007038 · Model: 400275 · ZYNEX MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NeuroMove
Primary DI
00852670007038
Version / Model
400275
Company Name
ZYNEX MEDICAL, INC.
Labeler DUNS
141582226
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-28
Public Version
3
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
b81fd52c-9474-48cd-900e-3fc3db65646d

Device Description

EMG-triggered NeuroMuscular stimulator to aid in stroke recovery

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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IPF Stimulator, Muscle, Powered
HCC Device, Biofeedback

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00852670007038

Customer Contacts

Phone
800-495-6670

Premarket Submissions

Submission Number Supplement Number
K012885 000