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Apteczka Euro Farma

by Grażyna Krówczyńska Firma Produkcyjno-Handlowa Grawena 2 variants

Ref 5908223900150

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59082239EUFA150LD Basic UDI-DI 05908223900150UDI-DIDate28 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
5908223900150
Primary DI / UDI-DI
05908223900150
Basic UDI-DI
59082239EUFA150LD
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
Zestaw przeznaczony do udzielenia pierwszej pomocy

Manufacturer details

EUDAMED SRN
PL-PR-000043423

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Properties

Other properties (1)

  • Sterile: No