← Back to catalogue

MedK Manifold Sets

EUDAMED

Class IIa (EU MDR)

Ref 982503RN010200Model MedK Manifold Sets

by medK GmbH

Identity

Device Name
MedK Manifold Sets EUDAMED
Model / Reference
MedK Manifold Sets EUDAMED
982503RN010200 EUDAMED

Identifiers

Primary DI / UDI-DI
+B827982503RN0102001 EUDAMED
Basic UDI-DI
B-+B827982503RN0102001 EUDAMED
EMDN Code
A0702 RAMPS 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

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

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
medK GmbH
EUDAMED SRN
DE-MF-000006273

Sources (1)

  • EUDAMED a2d7ee85-cd91-4412-bf34-15ebcb2d4108 61 fields · synced Jul 11, 2026