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Pneuven Medi 6.7

by EKOVUK MEDI, s.r.o. Czechia EUDAMED

Ref Pneuven Medi EMDN C0180

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859421244PNEUVEN27 Basic UDI-DIDate13 Mar 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
pneuven medi
Model / Reference
Pneuven Medi
Primary DI / UDI-DI
08594212440010
Basic UDI-DI
859421244PNEUVEN27
Direct Marketing DI
08594212440010
EMDN Code
C0180 Artero-venous system devices - accessories not included in other classes
Device Class
Class IIa
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000040403

Other devices from EKOVUK MEDI, s.r.o.

See all devices from EKOVUK MEDI, s.r.o. →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED d63256d7-c3a0-4ebc-9ddd-edb26d95783f 61 fields · synced 22 Oct 2026