FDA UDI In Commercial Distribution 🇺🇸 United States

MediMax Tech

DI: 00817325023399 · Model: MXF47T-50 · MEDIMAX TECH INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
MediMax Tech
Primary DI
00817325023399
Version / Model
MXF47T-50
Company Name
MEDIMAX TECH INC.
Labeler DUNS
927071162
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-10
Public Version
1
Public Version Date
2018-11-12
Public Version Status
New
Public Device Record Key
4ef17117-fe8a-474a-8fcc-0d9c2f67b4c1

Device Description

Electrode, Foam, 47mm, Teardrop, 50pc per pack

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
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
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 20817325023393
Package 10817325023396
Primary 00817325023399

Customer Contacts

Phone
855-633-4629

Premarket Submissions

Submission Number Supplement Number
K020003 000