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Map-iT Diagnostic Mapping Catheter Extension Cable

by Access Point Technologies EP Inc. 2 variants

Ref 901952

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number081808301EXTCABLEST Basic UDI-DI 00818083012793UDI-DIDate28 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Map-iT Extension Cable
Model / Reference
901952
Primary DI / UDI-DI
00818083012793
Basic UDI-DI
081808301EXTCABLEST
EMDN Code
C020380 Ablation of arrhythmogenic focus devices - accessories
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
US-MF-000011741
Authorised representative
S4M EUROPE FR-AR-000000180

Other devices from Access Point Technologies, Ep Inc.

See all devices from Access Point Technologies, Ep Inc. →

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