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Punzon Con Guia

by Ivalmed S.L.

Ref IVP-78-GUIDEDAWL

Active European Union

CE MDR

Valid until

30 Mar 2031

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number84357608INSPERFORACION7M Basic UDI-DI 08435760845332UDI-DIDate10 Apr 2024RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • ES26/00000408 Active

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    30 Mar 2026
    Expires
    30 Mar 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Instrumentos De Perforacion
Model / Reference
IVP-78-GUIDEDAWL
Primary DI / UDI-DI
08435760845332
Basic UDI-DI
84357608INSPERFORACION7M
Direct Marketing DI
08435760845332
EMDN Code
L0399 General surgery instruments, reusable - other
Device Class
Class I
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000000634

Other devices from Ivalmed S.L.

See all devices from Ivalmed S.L. →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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