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Болнично Реанимационно Легло За Интензивни Грижи С Антидекубитален Дюшек

by Ams Ood

Ref Isospace ICB-P-011

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 Number3800502369011S6 Basic UDI-DI 03800502369011UDI-DIDate10 Jul 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  • Withdrawn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
Hospital Intensive Care Bed with Anti-Decubitus Mattress
Model / Reference
Isospace ICB-P-011
Primary DI / UDI-DI
03800502369011
Basic UDI-DI
3800502369011S6
Direct Marketing DI
03800502369011
EMDN Code
V08060102 Intensive care or resuscitation electric medical beds
Device Class
Class I
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
BG-MF-000044546

Other devices from Ams Ood

See all devices from Ams Ood →

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