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Xenamed Industries

EUDAMED

Class I (EU MDR)

Ref 167-002

by Xenamed Industries

Identity

Trade Name
Xenamed Industries EUDAMED
Device Name
VAGINAL SPECULUMS EUDAMED
Model / Reference
167-002 EUDAMED

Identifiers

Primary DI / UDI-DI
+G2371670020% EUDAMED
Basic UDI-DI
++G237VaginalSpeculumsBC EUDAMED
EMDN Code
L059001 VAGINAL 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

Category: Vaginal speculum, reusable

Xenamed Industries by Xenamed Industries — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal speculum, reusable.

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 99954835-0a28-4a1a-a604-8bb9cd45745a 61 fields · synced Jun 18, 2026