FDA UDI In Commercial Distribution 🇺🇸 United States

MediMax Tech

DI: 00817325020398 · Model: MF2409 Surface Electrodes · MEDIMAX TECH INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MediMax Tech
Primary DI
00817325020398
Version / Model
MF2409 Surface Electrodes
Company Name
MEDIMAX TECH INC.
Labeler DUNS
927071162
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-19
Public Version
4
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
5868710f-16ed-4443-9190-c1116950d095

Device Description

MF2409: Ring, Surface EMG Electrodes, Pet Film, 8x107mm, Hydrogel

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
59692 Neuromuscular transmission motion sensor

Identifiers

Type ID
Package 20817325020392
Package 10817325020395
Primary 00817325020398

Customer Contacts

Phone
855-633-4629

Premarket Submissions

Submission Number Supplement Number
K153019 000