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ENT treatment unit MODULA Europa

EUDAMED

Class IIa (EU MDR)

Ref 0100-30000Model Duo

by Heinemann HNO Medizintechnik GmbH

Identity

Trade Name
ENT treatment unit MODULA Europa EUDAMED
Device Name
ENT treatment unit MODULA EUDAMED
Model / Reference
Duo EUDAMED
0100-30000 EUDAMED

Identifiers

Primary DI / UDI-DI
04262512210025 EUDAMED
Basic UDI-DI
0426251221MODW2 EUDAMED
EMDN Code
Q0399 ENT 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

ENT treatment unit MODULA Europa by Heinemann HNO Medizintechnik 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

EUDAMED SRN
DE-MF-000046391

Sources (1)

  • EUDAMED 1a614c36-6922-4337-9fe4-b3e13a91ac00 61 fields · synced Jul 21, 2026