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Autolékárnička velikost II. CZ, náhradní balíček č. III

by AGBA, v.o.s.

Ref 999100083Model Autolékárnička velikost II. CZ

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859402080lekarnaII22 Basic UDI-DI 08594020800785UDI-DIDate16 Apr 2025RegisteredStatusActive

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  • Withdrawn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
Autolékárnička velikost II. CZ, 999100083
Primary DI / UDI-DI
08594020800785
Basic UDI-DI
859402080lekarnaII22
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
Pro poskytnutí dočasné první předlékařské pomoci při nehodě

Manufacturer details

EUDAMED SRN
CZ-PR-000047388

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Properties

Other properties (1)

  • Sterile: No