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HYPROMELOZA-P® kapi za oko, otopina

by Unimed Pharma spol. s r.o.

Ref 11Model 1x10 ml

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 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/MDR Number8588009045HYPROMELOZAPR3 Basic UDI-DIDate17 Nov 2025RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
HYPROMELOZA-P eye drops, solution
Model / Reference
1x10 ml, 11
Primary DI / UDI-DI
08588009045212
Basic UDI-DI
8588009045HYPROMELOZAPR3
Direct Marketing DI
08588009045212
EMDN Code
Q02030206 Eye lubricant solutions
Device Class
Class IIb
Market of Registration
Croatia

Manufacturer details

EUDAMED SRN
SK-MF-000003111

Other devices from Unimed Pharma spol. s r.o.

See all devices from Unimed Pharma spol. s r.o. →

Properties

  • Sterile

Other properties (12)

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