Skip to content

Idroflog

by Alfa Intes Industria Terapeutica Splendore S.r.l. 16 variants

Ref 5010129

Active European Union

CE MDR

Valid until

13 Jun 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier ISTITUTO SUPERIORE DI SANITA'

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 NumberCSQ0023240326 Date3 Jul 2026IssuedStatusActive expires 13 Jun 2029

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • CSQ0023240326 Active Supplemented

    Quality management system EU MDR

    Issued
    3 Jul 2026
    Expires
    13 Jun 2029
    Reason
    Add device or group
  • CVD0028240125 Active Supplemented

    Technical documentation EU MDR

    Issued
    26 May 2025
    Expires
    13 Jun 2029
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
5010129
Primary DI / UDI-DI
08058481370367
Basic UDI-DI
805848137IDROFLOGAM
EMDN Code
Q02030206 Eye lubricant solutions
Device Class
Class III
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
IT-MF-000025980

Other devices from Alfa Intes Industria Terapeutica Splendore S.r.l.

  • Idroflog

    Class III
  • Oftaial

    Class IIb
  • Oftaial Plus

    Class IIb
  • Idroflog

    Class III
  • Idroflog

    Class III
  • Oftaial Plus

    Class IIb

See all devices from Alfa Intes Industria Terapeutica Splendore S.r.l. →

Properties

  • Sterile
  • Incorporates Medicinal Product

Other properties (11)

  • 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