FDA UDI In Commercial Distribution 🇺🇸 United States

MyoWorx

DI: 00628942249600 · Model: TM20 · MyoWorx Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MyoWorx
Primary DI
00628942249600
Version / Model
TM20
Company Name
MyoWorx Inc
Labeler DUNS
243202161
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-30
Public Version
1
Public Version Date
2023-06-07
Public Version Status
New
Public Device Record Key
e6847832-724a-4763-afc4-0de44ed62b74

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
IPF Stimulator, Muscle, Powered

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00628942249600

Premarket Submissions

Submission Number Supplement Number
K192746 000