FDA UDI In Commercial Distribution 🇺🇸 United States

MyndMove

DI: 00692520101659 · Model: MyndMove FES Stimulator · MyndTec Inc
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MyndMove
Primary DI
00692520101659
Version / Model
MyndMove FES Stimulator
Catalog Number
910165
Company Name
MyndTec Inc
Labeler DUNS
203019245
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-11
Public Version
4
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
d8198a2a-2845-466d-83c6-ae76ad07a76f

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
GZI Stimulator, Neuromuscular, External Functional

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00692520101659

Premarket Submissions

Submission Number Supplement Number
K170564 000