FDA UDI In Commercial Distribution 🇺🇸 United States

miha bodytec

DI: 04260646650014 · Model: miha bodytec m.ove · miha bodytec GmbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
miha bodytec
Primary DI
04260646650014
Version / Model
miha bodytec m.ove
Company Name
miha bodytec GmbH
Labeler DUNS
551434728
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-05
Public Version
2
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
529d1af0-3349-4d9d-b1b9-1ed1e65a39e7

Device Description

miha bodytec m.ove is a device which performs electronic muscle stimulation based on EMS technology. The device is specifically designed as an addition to other sports and for training muscles.

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NGX Stimulator, Muscle, Powered, For Muscle Conditioning
IPF Stimulator, Muscle, Powered

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 04260646650014

Premarket Submissions

Submission Number Supplement Number
K221498 000