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ezPad MRI (S)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 5300202

by MIPM Mammendorfer Institut für Physik und Medizin GmbH

Identity

Trade Name
ezPad MRI (S) EUDAMED
ezPad MRI FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
ezPadMRI - MRI ECG Electrode EUDAMED
MRI ECG Electrode 70mm x 70mm FDA UDI
Model / Reference
5300202 EUDAMED
small FDA UDI
Description
MRI ECG Electrode 70mm x 70mm FDA UDI

Identifiers

Catalog Number
5300202 FDA UDI
Primary DI / UDI-DI
04255629200300 EUDAMEDFDA UDI
Basic UDI-DI
42556292001013LW EUDAMED
FDA Product Code
DRX FDA UDI
EMDN Code
C020501 ECG ELECTRODES EUDAMED
GMDN Term
Electrocardiographic electrode, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.2360 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Electrocardiographic electrode, single-use

ezPad MRI (S) by MIPM Mammendorfer Institut für Physik und Medizin GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
DE-MF-000007654

Sources (2)

  • EUDAMED badcad82-0393-445b-9011-c5623e1cddf0 61 fields · synced Jun 19, 2026
  • FDA UDI dc532982-5203-43ff-b6fc-dcc6e9341202 36 fields · synced May 30, 2026