Skip to content

Alegio™ NG

by Invacare Portugal, Unipessoal Lda. 30 variants

Ref 1608537-7035

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5600494ALEGIONGTQ Basic UDI-DI 05600494125675UDI-DIDate18 Dec 2025RegisteredStatusActive

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  • Withdrawn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
Alegio NG
Model / Reference
1608537-7035
Primary DI / UDI-DI
05600494125675
Basic UDI-DI
5600494ALEGIONGTQ
EMDN Code
V08060101 Hospital/home care electric medical beds
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000006551

Other devices from Invacare Portugal, Unipessoal Lda.

See all devices from Invacare Portugal, Unipessoal Lda. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No