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SoreFix Rescue cold sore cream - 6 mL Tube

by Serrix B.V

Ref L040IE

Active European Union

CE MDR

Valid until

19 Jun 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberBE23/00000172 Date9 Jul 2026IssuedStatusActive expires 19 Jun 2028

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • BE23/00000172 Active

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    9 Jul 2026
    Expires
    19 Jun 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
SoreFix lip balm
Model / Reference
L040IE
Primary DI / UDI-DI
08718309701345
Basic UDI-DI
871830970L0X0EGBT
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
NL-MF-000005882

Other devices from Serrix B.V

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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