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vMap

by Vektor Medical Inc.

Ref 714-00001

vMap (714-00001) is a Class IIa device made by Vektor Medical, Inc., registered in EUDAMED on 26 May 2026 (Basic UDI-DI 00860007954DP-1000vMapBD), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number00860007954DP-1000vMapBD Basic UDI-DI 00860007954153UDI-DIDate26 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Vektor Computational ECG Mapping System (vMap)
Model / reference
714-00001
Primary DI / UDI-DI
00860007954153
Basic UDI-DI
00860007954DP-1000vMapBD
EMDN code
C020199 Cardiac electrophysiology and mapping devices - other
Device class
Class IIa
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
US-MF-000047086
Authorised representative
Veranex Germany GmbH DE-AR-000005578

Similar devices in this category

Other devices filed under CARDIAC ELECTROPHYSIOLOGY AND MAPPING DEVICES - OTHER.

Other devices from Vektor Medical, Inc.

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Properties

Other properties (14, all answered No)