FDA UDI In Commercial Distribution 🇺🇸 United States

MediMax Tech

DI: 00817325020596 · Model: CF50R Tens Electrode · MEDIMAX TECH INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
MediMax Tech
Primary DI
00817325020596
Version / Model
CF50R Tens Electrode
Company Name
MEDIMAX TECH INC.
Labeler DUNS
927071162
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-03
Public Version
3
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
bbd6bce4-7291-49bf-91b3-e6cf86326adf

Device Description

CF50R Tens Electrode - Standard Foam 48mm Round Stimulating Electrodes

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXY Electrode, Cutaneous

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Package 30817325020597
Package 20817325020590
Package 10817325020593
Primary 00817325020596

Customer Contacts

Phone
855-633-4629