← Back to catalogue

Artemis

EUDAMED

Class I (EU MDR)

Ref ArtemisModel Artemis、Artemis/M

by Mediland Enterprise Corporation

Identity

Trade Name
Artemis EUDAMED
Device Name
Artemis Series Electric Surgical Table EUDAMED
Model / Reference
Artemis、Artemis/M EUDAMED
Artemis EUDAMED

Identifiers

Primary DI / UDI-DI
04719879260908 EUDAMED
Basic UDI-DI
471987926ArtemisAA EUDAMED
EMDN Code
Z12011202 OPERATING TABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Artemis by Mediland Enterprise Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
TW-MF-000012153
Authorised Representative
Luana Med. B.V. NL-AR-000002750

Sources (1)

  • EUDAMED ec19f3a2-b655-4881-a8a3-603dfbd5f254 61 fields · synced Jun 18, 2026