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Spéculum nasal

EUDAMED

Class I (EU MDR)

Ref 8001623

by Applimed SA

Identity

Device Name
Spéculum nasal EUDAMED
Model / Reference
8001623 EUDAMED

Identifiers

Primary DI / UDI-DI
07640178436503 EUDAMED
Basic UDI-DI
B-07640178436503 EUDAMED
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Spéculum nasal by Applimed SA — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Applimed SA
EUDAMED SRN
CH-MF-000046641
Authorised Representative
Dansu A/S DK-AR-000046254

Sources (1)

  • EUDAMED 712c8d2a-1159-48f0-87c7-55971cd49edb 61 fields · synced Jun 20, 2026