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MedK Introducer Sets

EUDAMED

Class IIa (EU MDR)

Ref 982118F2122Model MedK Introducer Sets

by medK GmbH

Identity

Device Name
MedK Introducer Sets EUDAMED
Model / Reference
MedK Introducer Sets EUDAMED
982118F2122 EUDAMED

Identifiers

Primary DI / UDI-DI
+B827982118F21221 EUDAMED
Basic UDI-DI
B-+B827982118F21221 EUDAMED
EMDN Code
C0504 ARTERIAL INTRODUCTION SETS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Category: Interventional radiology percutaneous-access kit, single-use

MedK Introducer Sets by medK GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Interventional radiology percutaneous-access kit, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
medK GmbH
EUDAMED SRN
DE-MF-000006273

Sources (1)

  • EUDAMED b5dd5d68-8c2d-4946-b042-9aa8dfc1c097 61 fields · synced Jul 22, 2026