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Adapta™ Mvp™

by Medtronic, Inc. 2 variants

Ref ADDR01

Adapta™ Mvp™ (ADDR01) is a device classified as Active implantable (AIMDD) made by Medtronic, Inc., registered in EUDAMED on 2 Sep 2026 (Basic UDI-DI B-00613994223838), active as of 25 Oct 2026.

Active European Union

CE AIMDD

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/AIMDD NumberB-00613994223838 Basic UDI-DI Date2 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/AIMDD Active

Specification

EUDAMED

Device name
Adapta, Versa Sensia Relia Ipg
Model / reference
ADDR01
Primary DI / UDI-DI
00613994223838, 00613994558510, 00885074498836, 00613994741707
Basic UDI-DI
B-00613994223838, B-00613994558510, B-00885074498836, B-00613994741707
EMDN code
J01010302 Implantable dual chamber pacemakers with sensor (dr)
Device class
Class AIMDD
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 IMPLANTABLE PACEMAKERS.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)