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Aster Recliner Manual Cadet Zest 117 Royal

by Reha-Bed Sp. z o.o.

Ref FTL/A1/45, L1SM1120S0L060200S00T01I06Model LEO

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59041832ASTERMR Basic UDI-DI 05904183216607UDI-DIDate19 Nov 2025RegisteredStatusActive

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  • Withdrawn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

Trade Name
Aster Recliner Manual Cadet Zest 117 Royal
Leo
Device Name
Aster
Model / Reference
FTL/A1/45, LEO, L1SM1120S0L060200S00T01I06
Primary DI / UDI-DI
05904183216607
Basic UDI-DI
59041832ASTERMR, 59041832LEOXT
Direct Marketing DI
05904183216607
EMDN Code
V080202, V08060101
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000040289

Other devices from Reha-Bed Sp. z o.o.

See all devices from Reha-Bed Sp. z o.o. →

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