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Detroit

by REBOTEC Rehabilitationsmittel GmbH

Ref 3643012, 3645412, 3640312Model Dusch-Toilettenrollstühle

Detroit (3643012) is a Class I device made by REBOTEC Rehabilitationsmittel GmbH, registered in EUDAMED on 15 Mar 2024 (Basic UDI-DI 4046678_STDTSx-0012-150KQ), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4046678_STDTSx-0012-150KQ Basic UDI-DI Date15 Mar 2024RegisteredStatusActive

Official records

  • EUDAMED public site Basic UDI-DI 4046678_STDTSx-0012-150KQ — open Devices and search for it

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  • Withdrawn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
Dusch-Toilettenrollstühle, 3643012, 3645412, 3640312
Primary DI / UDI-DI
04046678013108, 04046678013115, 04046678013092
Basic UDI-DI
4046678_STDTSx-0012-150KQ
Direct marketing DI
04046678013108
04046678013115
04046678013092
EMDN code
Y091203 Chairs, toilet and shower
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000009447

Similar devices in this category

Other devices filed under CHAIRS, TOILET AND SHOWER.

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Properties

Other properties (14, all answered No)