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medilogFD

EUDAMED

Class IIa (EU MDR)

Ref 3.900491Model medilogFD

by Schiller Ag

Identity

Trade Name
medilogFD EUDAMED
Device Name
medilogFD EUDAMED
Model / Reference
medilogFD EUDAMED
3.900491 EUDAMED

Identifiers

Primary DI / UDI-DI
07613365004007 EUDAMED
Basic UDI-DI
761336500000002254 EUDAMED
Direct Marketing DI
07613365004007 EUDAMED
EMDN Code
Z12050403 ECG HOLTER RECORDERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

medilogFD 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 8e0777a1-3098-4db3-aed8-8bef0f3d91bf 61 fields · synced Jul 8, 2026