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Amax9800

by Mediland Enterprise Corporation

Ref Amax9800Model Amax9800、Artemis、Amax9000

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471987926Amax98009J Basic UDI-DI 04719879261301UDI-DIDate24 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Amax9800 Series Electric Surgical Table
Model / Reference
Amax9800、Artemis、Amax9000, Amax9800
Primary DI / UDI-DI
04719879261301
Basic UDI-DI
471987926Amax98009J
EMDN Code
Z12011202 Operating tables
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

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

Other devices from Mediland Enterprise Corporation

See all devices from Mediland Enterprise Corporation →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No