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Geneo

by PROMA REHA, s.r.o.

Part of a family of 22 devices: see the family page

Ref GENEO

Geneo is a Class I device made by PROMA REHA, s.r.o., registered in EUDAMED on 26 May 2026 (Basic UDI-DI 859420232LP01EP), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859420232LP01EP Basic UDI-DI 85942023205370UDI-DIDate26 May 2026RegisteredStatusActive

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  • Withdrawn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

Device name
Kinetic bed
Model / reference
GENEO
Primary DI / UDI-DI
85942023205370
Basic UDI-DI
859420232LP01EP
Direct marketing DI
85942023205370
EMDN code
V08060101 Hospital/home care electric medical beds
Device class
Class I
EU registration type
Standard device
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000013860

Similar devices in this category

Other devices filed under HOSPITAL/HOME CARE ELECTRIC MEDICAL BEDS.

Other devices from PROMA REHA, s.r.o.

See all devices from PROMA REHA, s.r.o. →

Properties

Other properties (14, all answered No)