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Yurway® Medikamentenkartusche

by NeuroDerm Ltd.

Ref MS000684

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7290017498NDMC001EH Basic UDI-DI 07290017498263UDI-DIDate24 May 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  • Withdrawn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
Yurway® Medication Cartridge
Model / Reference
MS000684
Primary DI / UDI-DI
07290017498263
Basic UDI-DI
7290017498NDMC001EH
EMDN Code
A020199 Syringes, single-use - other
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000042765
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Other devices from NeuroDerm Ltd.

See all devices from NeuroDerm Ltd. →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

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