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Gseba Mousse

by Laboratori Farmaceutici Krymi SpA

Ref 11

Active European Union

CE MDR

Valid until

17 Sep 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ISTITUTO SUPERIORE DI SANITA'

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCSQ0038260226 Date18 Sep 2026IssuedStatusActive expires 17 Sep 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • CSQ0038260226 Active Supplemented

    Quality management system EU MDR

    Certifier
    ISTITUTO SUPERIORE DI SANITA' 0373
    Issued
    18 Sep 2026
    Expires
    17 Sep 2031
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
11
Primary DI / UDI-DI
08058450781392
Basic UDI-DI
805845078113FH
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
IT-MF-000029024

Other devices from Laboratori Farmaceutici Krymi SpA

  • Kromic

    Class III

  • Gseba Cream

    Class IIa

Properties

Other properties (13)

  • Sterile: No
  • 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