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Rf Marinr™

by Medtronic, Inc. 7 variants

Ref 076514

Rf Marinr™ (076514) is a Class III device made by Medtronic, Inc., registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-00643169883826), active as of 7 Nov 2026.

Active European Union

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00643169883826 Basic UDI-DI 00643169883826UDI-DIDate6 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Ablation Catheters
Model / reference
076514
Primary DI / UDI-DI
00643169883826
Basic UDI-DI
B-00643169883826
EMDN code
C020301 Arrhythmogenic foci radiofrequency ablation catheters
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000019977
Authorised representative
Medtronic B.V. NL-AR-000006050

Similar devices in this category

Other devices filed under CARDIAC TISSUE ABLATION DEVICES.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Supplied sterile
Other properties (13, all answered No)