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ZUMA n·oka + ulga dla oczu 0,1 - ZUMA n·oka + ulga dla oczu 0, 1

by SUPROBION Sp. z o.o.

Ref 12394_PLModel Lubricating eye drops with sodium hyaluronate 0,1% and eyebright herb extract

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-05900741962054 Basic UDI-DI 05900741962054UDI-DIDate23 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
Lubricating eye drops with sodium hyaluronate 0, 1% and eyebright herb extract, 12394_PL
Primary DI / UDI-DI
05900741962054
Basic UDI-DI
B-05900741962054
EMDN Code
Q02030206 Eye lubricant solutions
Models / Variants
ZUMA n·oka + ulga dla oczu 0, 1
Device Class
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000018264

Other devices from SUPROBION Sp. z o.o.

See all devices from SUPROBION Sp. z o.o. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No