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ATMOS Video Otoskop V2

EUDAMED

Class I (EU MDR)

Ref ATMOS Video Otoskop V2Model OX2

by Orlvision GmbH

Identity

Trade Name
ATMOS Video Otoskop V2 EUDAMED
Device Name
Otoskop OX2 EUDAMED
Model / Reference
OX2 EUDAMED
ATMOS Video Otoskop V2 EUDAMED

Identifiers

Primary DI / UDI-DI
04260499410230 EUDAMED
Basic UDI-DI
426049941OTOLL EUDAMED
Direct Marketing DI
04260499410230 EUDAMED
EMDN Code
Z12021009 DIRECT OUTPATIENT VIDEO-OTOSCOPES 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

ATMOS Video Otoskop V2 by orlvision 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
Orlvision GmbH
EUDAMED SRN
DE-MF-000013894

Sources (1)

  • EUDAMED 2947bfa0-cfe2-4afe-9776-ad15b63f9bd0 61 fields · synced Jun 19, 2026