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Dk50 De

EUDAMED

Class IIb (EU MDR)

Ref 430402009-313Model DK50 DE

by EKOM spol. s r.o.

Identity

Trade Name
DK50 DE EUDAMED
Device Name
Medical compressor EUDAMED
Model / Reference
DK50 DE EUDAMED
430402009-313 EUDAMED

Identifiers

Primary DI / UDI-DI
08586014621551 EUDAMED
Basic UDI-DI
B-08586014621551 EUDAMED
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Slovakia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Pulmonary function analysis system, adult

Dk50 De by EKOM spol. s r.o. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function analysis system, adult.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
EKOM spol. s r.o.
EUDAMED SRN
SK-MF-000002069

Sources (1)

  • EUDAMED 770962b6-893d-447c-baff-fc607d58faa6 61 fields · synced Jul 8, 2026