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F2017

EUDAMEDFDA UDI

Class I (EU MDR)

Ref F2017Model Disposable electrodes for ECG

by FIAB S.p.A.

Identity

Trade Name
NA FDA UDI
Generic Name
Electrocardiographic electrode, single-use FDA UDI
Device Name
Disposable round-shaped ECG electrodes with liquid gel, Ø 50mm, Silver/Silver Chloride(SSC) sensor and metal snap. These electrodes are suitable for short and medium term monitoring, stress ECG recording and Holter, with a direct application onto the skin. The SSC sensor permits a reliable and stable recording and off-centered configuration allows a better quality of ECG signal and reduces artifacts. FDA UDI
Model / Reference
Disposable electrodes for ECG EUDAMED
F2017 EUDAMEDFDA UDI
Description
Disposable round-shaped ECG electrodes with liquid gel, Ø 50mm, Silver/Silver Chloride(SSC) sensor and metal snap. These electrodes are suitable for short and medium term monitoring, stress ECG recording and Holter, with a direct application onto the skin. The SSC sensor permits a reliable and stable recording and off-centered configuration allows a better quality of ECG signal and reduces artifacts. FDA UDI

Identifiers

Catalog Number
F2017 FDA UDI
Primary DI / UDI-DI
08054953341224 EUDAMEDFDA UDI
Basic UDI-DI
803300326608000001SB 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
Italy 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

No

FDA UDI

F2017 by FIAB S.p.A. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FIAB S.p.A.
EUDAMED SRN
IT-MF-000005988

Sources (2)

  • EUDAMED 44fecf75-482b-459c-b00b-c57b058a948e 61 fields · synced Jul 16, 2026
  • FDA UDI cd006ee0-1c5b-4f46-8eeb-77ddaaa58888 36 fields · synced May 29, 2026