Skip to content

Aster

by Reha-Bed Sp. z o.o. 37 variants

Part of a family of 75 devices: see the family page

Ref FTL/A1/118

Aster (FTL/A1/118) is a Class I device made by Reha-Bed Sp. z o.o., registered in EUDAMED on 19 Nov 2025 (Basic UDI-DI 59041832ASTERMR), 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 Number59041832ASTERMR Basic UDI-DI 05904183225012UDI-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  • Withdrawn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/A1/118
Primary DI / UDI-DI
05904183225012
Basic UDI-DI
59041832ASTERMR
Direct marketing DI
05904183225012
EMDN code
V080202 Manual 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 MANUAL 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)