Skip to content

Posodica 80ml zaskočni pokrov

by Golias d.o.o.

Ref PO41Model Posodica 80ml zaskočni pokrov

Active European Union

CE IVDR

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/IVDR Number383003667CON80PUSHCAPAC Basic UDI-DI 03830036670017UDI-DIDate21 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / Reference
Posodica 80ml zaskočni pokrov, PO41
Primary DI / UDI-DI
03830036670017
Basic UDI-DI
383003667CON80PUSHCAPAC
EMDN Code
W050180 Samples collection devices - other accessories
Device Class
Class A
EU market of registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000006917

Other devices from Golias d.o.o.

See all devices from Golias d.o.o. →

Properties

  • Professional Testing

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No