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Set pour Hémodialyse Standard

by Medirm - Fabrico e Comércio de Dispositivos Médicos

Ref 2110000800

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number560089748551ER Basic UDI-DI 05600897482269UDI-DIDate12 Oct 2026RegisteredStatusActive EUDAMED: not on the EU market

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Haemodialysis Set
Model / Reference
2110000800
Primary DI / UDI-DI
05600897482269
Basic UDI-DI
560089748551ER
EMDN Code
F0303 Haemodialysis kits
Device Class
Class IIa
Medical Purpose
The Haemodialysis Set is intended to provide the necessary components to support the preparation and performance of haemodialysis procedures. The set is intended for use by healthcare professionals in clinical settings.

Manufacturer details

EUDAMED SRN
PT-PR-000002819

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Properties

  • Sterile