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Rhinoscopes

EUDAMED

Class IIa (EU MDR)

Ref 8300060563

by Henke-Sass, Wolf GmbH

Identity

Trade Name
RHINOSCOPES EUDAMED
Device Name
Sinuscope EUDAMED
Model / Reference
8300060563 EUDAMED

Identifiers

Primary DI / UDI-DI
04035873072423 EUDAMED
Basic UDI-DI
403587312010109A8 EUDAMED
Direct Marketing DI
04035873072423 EUDAMED
EMDN Code
Z12021008 RHINOSCOPES 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

Rhinoscopes by Henke-Sass, Wolf 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-000005531

Sources (1)

  • EUDAMED 69acff73-ccb1-4fbe-8195-402b3102dd69 61 fields · synced Jun 17, 2026