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Anasthesie Tupfer Pack

by Medirm - Fabrico e Comércio de Dispositivos Médicos 2 variants

Ref 2110000840Model Anaesthesia sets

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number560089748558F7 Basic UDI-DI 05600897481958UDI-DIDate13 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  • Withdrawn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

Model / Reference
Anaesthesia sets, 2110000840
Primary DI / UDI-DI
05600897481958
Basic UDI-DI
560089748558F7
EMDN Code
T0203 Dressing and assistance kits
Device Class
Class IIa
Medical Purpose
The Anaesthesia Set is intended to provide the necessary components to support the preparation and performance of anaesthesia 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