← Back to catalogue

Disposable EZ-Trode ECG Electrodes

FDA UDI

Class II (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Disposable EZ-Trode ECG Electrodes FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
Midmark EZ-trode disposable tab ECG electrodes are designed to provide excellent conductivity and uniform current dispersion. FDA UDI
Model / Reference
2-100-0204 FDA UDI
Description
Midmark EZ-trode disposable tab ECG electrodes are designed to provide excellent conductivity and uniform current dispersion. FDA UDI

Identifiers

Catalog Number
2-100-0204 FDA UDI
Primary DI / UDI-DI
10841709100212 FDA UDI
FDA Product Code
DPS FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2340 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic electrode, single-use

Disposable EZ-Trode ECG Electrodes by Midmark Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI 3bc4eb9f-c387-4346-a6eb-f0893cfb528e 36 fields · synced Jun 8, 2026