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Omnipor

by Paul Hartmann AG Germany EUDAMED

Ref 900547Model 1691

EMDN M050199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40495001691L2 Basic UDI-DIDate5 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
1691, 900547
Primary DI / UDI-DI
04052199237398
Basic UDI-DI
40495001691L2
Unit of Use DI
04052199155883
EMDN Code
M050199 Surgical plasters - other
Device Class
Class I
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
DE-MF-000005861

Other devices from Paul Hartmann AG

See all devices from Paul Hartmann AG →

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 04052199237398|40495001691L2 61 fields · synced 24 Oct 2026