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Aster Electric

by Reha-Bed Sp. z o.o. 11 variants

Ref FTL/A2/118

Aster Electric (FTL/A2/118) is a Class I device made by Reha-Bed Sp. z o.o., registered in EUDAMED on 19 Nov 2025 (Basic UDI-DI 59041832ASTERELSW), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59041832ASTERELSW Basic UDI-DI 05904183225029UDI-DIDate19 Nov 2025RegisteredStatusActive

Official records

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  • Withdrawn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

Model / reference
FTL/A2/118
Primary DI / UDI-DI
05904183225029
Basic UDI-DI
59041832ASTERELSW
Direct marketing DI
05904183225029
EMDN code
V08020101 Generic use electric medical chairs
Device class
Class I
EU registration type
Standard device
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000040289

Similar devices in this category

Other devices filed under GENERIC USE ELECTRIC MEDICAL CHAIRS.

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

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

Properties

Other properties (14, all answered No)