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Etos Kalknagelpen - 4 mL Pen

by Serrix B.V

Ref M630NL

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 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  • Withdrawn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
Nail Repair
Model / Reference
M630NL
Primary DI / UDI-DI
08710198474935
Basic UDI-DI
871830970M6X0EGEA
EMDN Code
M0410 Dressings for nails in the form of liquids, gels and creams
Device Class
Class IIa
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000005882

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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