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EZ-Dop

EUDAMED

Class IIa (EU MDR)

Ref 9001Model EZ-Dop Series

by Compumedics Germany GmbH

Identity

Trade Name
EZ-Dop EUDAMED
Device Name
EZ-Dop K1 EUDAMED
Model / Reference
EZ-Dop Series EUDAMED
9001 EUDAMED

Identifiers

Primary DI / UDI-DI
04260493312738 EUDAMED
Basic UDI-DI
4260493319000VL EUDAMED
Direct Marketing DI
04260493312738 EUDAMED
EMDN Code
Z12040111 BLOOD FLOW METERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

EZ-Dop by Compumedics Germany GmbH — 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

EUDAMED SRN
DE-MF-000005586

Sources (1)

  • EUDAMED 30a8ef70-91d5-4e7d-8c29-7180cff97417 61 fields · synced Jul 19, 2026