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Nasopharyngoskop PED

EUDAMED

Class I (EU MDR)

Ref Nasopharyngoskop PED

by Orlvision GmbH

Identity

Trade Name
Nasopharyngoskop PED EUDAMED
Device Name
Video Rhino Laryngoskop EUDAMED
Model / Reference
Nasopharyngoskop PED EUDAMED

Identifiers

Primary DI / UDI-DI
04260499410049 EUDAMED
Basic UDI-DI
426049941VRLMB EUDAMED
Direct Marketing DI
04260499410049 EUDAMED
EMDN Code
Z12021006 VIDEO NASOPHARYNGO/LARYNGOSCOPES 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

Yes

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

Nasopharyngoskop PED 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 ce610e26-a16b-46bc-acab-ee0541d06e18 61 fields · synced Jun 19, 2026