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Recording and stimulating for central nervous system electrodes

by Spes Medica S.p.A. Italy EUDAMED

Ref IEP0009 EMDN N99

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8054655000023Y2 Basic UDI-DIDate11 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 287/MDR Issued

    Technical documentation EU MDR

    Notified body
    Notified body 0051
    Issued
    5 Aug 2026
    Expires
    30 May 2028

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Platinum Grid Recording and Stimulating for Central Nervous System electrodes
Model / Reference
IEP0009
Primary DI / UDI-DI
18054655034506
Basic UDI-DI
8054655000023Y2
EMDN Code
N99 Nervous and medullary system devices - other
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000008858

Other devices from Spes Medica S.p.A.

See all devices from Spes Medica S.p.A. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Contains Latex
Other properties (11)
  • Implantable: No
  • Reusable: 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

Sources (1)

  • EUDAMED 18054655034506|8054655000023Y2 61 fields · synced 24 Oct 2026