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Temporäre Myokardiale Elektrode (TME)

by Neuromedex GmbH 5 variants

Ref 23.010211

Active European Union

CE MDR

Valid until

5 Jan 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DNV MEDCERT GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426002751110-128-1MS Basic UDI-DI 04260027517769UDI-DIDate29 Apr 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 10551GB450260311 Active Reissued

    Technical documentation EU MDR

    Certifier
    DNV MEDCERT GmbH 0482
    Issued
    11 Mar 2026
    Expires
    5 Jan 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Temporary Myocardial Electrode (TME)
Model / Reference
23.010211
Primary DI / UDI-DI
04260027517769
Basic UDI-DI
426002751110-128-1MS
EMDN Code
Z12050603 Transthoracic cardiac stimulators
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005867

Other devices from Neuromedex GmbH

See all devices from Neuromedex GmbH →

Properties

  • Sterile

Other properties (12)

  • 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