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Xenamed Industries

EUDAMED

Class I (EU MDR)

Ref 089-002

by Xenamed Industries

Identity

Trade Name
Xenamed Industries EUDAMED
Device Name
NASAL SPECULUMS EUDAMED
Model / Reference
089-002 EUDAMED

Identifiers

Primary DI / UDI-DI
+G23708900202 EUDAMED
Basic UDI-DI
++G237NasalSpeculumsSHD EUDAMED
EMDN Code
L149004 ENT SPECULUMS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark 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

Xenamed Industries by Xenamed Industries — 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
Xenamed Industries
EUDAMED SRN
PK-MF-000037495
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 3a590bac-3f44-4437-a3c9-e80352ae658b 61 fields · synced Jun 18, 2026