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Viacell L310

by Viacell s.r.o.

Ref 1510.04

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 Number85940621400TD003WA Basic UDI-DI 08594062141136UDI-DIDate12 Aug 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  • Withdrawn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 první pomoci
Model / Reference
1510.04
Primary DI / UDI-DI
08594062141136
Basic UDI-DI
85940621400TD003WA
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
Lékárnička určená k poskytnutí první předlékařské pomoci.

Manufacturer details

EUDAMED SRN
CZ-PR-000051826

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Properties

Other properties (1)

  • Sterile: No