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Preparation-Set - sterile

by MEL Medical GmbH 40 variants

Ref 222011

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42558177AngiographyC2 Basic UDI-DI 04255817702852UDI-DIDate30 Sep 2026RegisteredStatusActive

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  • Withdrawn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
Angiography
Model / Reference
222011
Primary DI / UDI-DI
04255817702852
Basic UDI-DI
42558177AngiographyC2
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class IIb
Medical Purpose
Angiography

Manufacturer details

EUDAMED SRN
DE-PR-000042395

Other devices from MEL Medical GmbH

See all devices from MEL Medical GmbH →

Properties

  • Sterile