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POLY Mixing Pad

EUDAMED

Class I (EU MDR)

Ref 80901

by M. G. Kurth GmbH

Identity

Trade Name
POLY Mixing Pad EUDAMED
Device Name
Anmischblock EUDAMED
Model / Reference
80901 EUDAMED

Identifiers

Primary DI / UDI-DI
++G086809011 EUDAMED
Basic UDI-DI
++G086AnmischblocksDJ EUDAMED
Direct Marketing DI
++G086809011 EUDAMED
EMDN Code
Q010503 IMPRESSION MATERIAL TRAYS, SINGLE-USE EUDAMED

Classification

Device Class
Class I 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

POLY Mixing Pad by M. G. Kurth GmbH — Class I — 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
M. G. Kurth GmbH
EUDAMED SRN
DE-MF-000045501

Sources (1)

  • EUDAMED 5234a8f8-6f14-4f8d-a4fa-f7db5ec751b9 61 fields · synced Jun 11, 2026