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Vienna Nazal Specula Infant

EUDAMED

Class I (EU MDR)

Ref 41-104 RI

by Raydent Instruments

Identity

Trade Name
VIENNA NAZAL SPECULA INFANT EUDAMED
Device Name
VIENNA NAZAL SPECULA INFANT EUDAMED
Model / Reference
41-104 RI EUDAMED

Identifiers

Primary DI / UDI-DI
G26841104RI0 EUDAMED
Basic UDI-DI
++G26841104RIX4 EUDAMED
EMDN Code
L149004 ENT SPECULUMS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Vienna Nazal Specula Infant by Raydent Instruments — 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
Raydent Instruments
EUDAMED SRN
PK-MF-000032781
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 05d04dc7-519d-48e2-a481-11ceaba83377 61 fields · synced Jun 19, 2026