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Midmark IQholter® Electrodes

FDA UDI

Class II (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Midmark IQholter® Electrodes FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
Midmark IQholter® electrodes are designed with a stress loop system to reduce artifacts and extra adhesion to prevent accidental removal. FDA UDI
Model / Reference
2-100-0060 FDA UDI
Description
Midmark IQholter® electrodes are designed with a stress loop system to reduce artifacts and extra adhesion to prevent accidental removal. FDA UDI

Identifiers

Catalog Number
2-100-0060 FDA UDI
Primary DI / UDI-DI
10841709100687 FDA UDI
FDA Product Code
MLO FDA UDI
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2800 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

Midmark IQholter® 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

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Manufacturer

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI fbc6f52c-c82a-4f0d-882f-615782160358 36 fields · synced Jun 8, 2026