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Cardiovit Ft-2

EUDAMED

Class IIa (EU MDR)

Ref 3.900880Model CARDIOVIT FT-2

by Schiller Ag

Identity

Trade Name
CARDIOVIT FT-2 EUDAMED
Device Name
CARDIOVIT FT-2 EUDAMED
Model / Reference
CARDIOVIT FT-2 EUDAMED
3.900880 EUDAMED

Identifiers

Primary DI / UDI-DI
07613365003536 EUDAMED
Basic UDI-DI
76133650000000175B EUDAMED
Direct Marketing DI
07613365003536 EUDAMED
EMDN Code
Z12050301 GENERAL PURPOSE ELECTROCARDIOGRAPHS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Cardiovit Ft-2 by Schiller AG — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Schiller Ag
EUDAMED SRN
CH-MF-000012722
Authorised Representative
SCHILLER Medizintechnik GmbH DE-AR-000006934

Sources (1)

  • EUDAMED e6eb0b7a-5841-4628-84d0-1eb1973c810d 61 fields · synced Aug 4, 2026