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KDM Pure-Fluid

EUDAMED

Class IIa (EU MDR)

Ref 031113

by Alpro Medical Gmbh

Identity

Trade Name
KDM Pure-Fluid EUDAMED
Device Name
Alpron EUDAMED
Model / Reference
031113 EUDAMED

Identifiers

Primary DI / UDI-DI
+E2510311131 EUDAMED
Basic UDI-DI
++E251002103007D EUDAMED
Direct Marketing DI
+E2510311131 EUDAMED
EMDN Code
D0299 BIGUANIDES FOR THE DISINFECTION OF MEDICAL DEVICES - OTHER 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

KDM Pure-Fluid by Alpro Medical 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

Manufacturer
Alpro Medical Gmbh
EUDAMED SRN
DE-MF-000010603

Sources (1)

  • EUDAMED 221d4734-8d8e-46a9-b64e-472e119fa76d 61 fields · synced Oct 6, 2026