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Areste

by Invacare Portugal, Unipessoal Lda.

Ref L110

Areste (L110) is a Class I device made by Invacare Portugal, Unipessoal Lda., registered in EUDAMED on 18 Dec 2025 (Basic UDI-DI 5600494ARESTESU), 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 Number5600494ARESTESU Basic UDI-DI 05600494140968UDI-DIDate18 Dec 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  • Withdrawn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
L110
Primary DI / UDI-DI
05600494140968
Basic UDI-DI
5600494ARESTESU
EMDN code
V080699 Medical beds - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000006551

Similar devices in this category

Other devices filed under MEDICAL BEDS - OTHER.

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Properties

Other properties (14, all answered No)