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Diagnosis and Treatment Bed

by Shandong Deman Medical Equipment Group Co., LTD 5 variants

Ref AZ-4Model AZ-1、AZ-2、AZ-3、AZ-4、AZ-5

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697669681datb001A9 Basic UDI-DI 06976696816512UDI-DIDate8 Sep 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  • Withdrawn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
Diagnosis and Treatment Bed
Model / Reference
AZ-1、AZ-2、AZ-3、AZ-4、AZ-5, AZ-4
Primary DI / UDI-DI
06976696816512
Basic UDI-DI
697669681datb001A9
EMDN Code
V080603 Treatment, diagnosis and monitoring medical beds
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000037481
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Shandong Deman Medical Equipment Group Co., Ltd

See all devices from Shandong Deman Medical Equipment Group Co., Ltd →

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