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Autolékárnička typ II v textilním obalu

by STERIWUND spol. s r.o.

Ref 0538

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 Number85951541025VL Basic UDI-DI 08595154105166UDI-DIDate20 Jul 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  • Withdrawn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

Device Name
Lékárnička neléčebná - souprava pro první pomoc
Model / Reference
0538
Primary DI / UDI-DI
08595154105166
Basic UDI-DI
85951541025VL
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
For providing first aid in emergency situations and for the prompt initial treatment of injuries, in accordance with the intended purpose of the kit components. For single use only.

Manufacturer details

EUDAMED SRN
CZ-PR-000052691

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Properties

Other properties (1)

  • Sterile: No