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Evera MRI™ S VR SureScan® DVMC3D4

by Medtronic, Inc.

Ref DVMC3D4

Active European Union. Also listed in GUDID (US), not in commercial distribution.

CE MDD CE AIMDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

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

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/AIMDD EUDAMED NumberB-00763000206208 Basic UDI-DI Date25 Aug 2026RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-00763000206208 Basic UDI-DI Date25 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00763000206208 UDI-DI Date13 Nov 2020ListedStatusListed GUDID: not in commercial distribution

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

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/AIMDD, CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Evera MRI™ S VR SureScan™ EUDAMED
Evera MRI™ S VR SureScan® GUDID
Generic Name
Single-chamber implantable defibrillator
Device Name
Evera,Visia AF, Primo/Mirro w MRI
Model / Reference
DVMC3D4
Primary DI / UDI-DI
00763000206208 EUDAMED
00643169649347 EUDAMED
00643169314207 EUDAMED
00643169720602 EUDAMED
00643169720589 GUDID
Basic UDI-DI
B-00763000206208, B-00643169649347, B-00643169314207, B-00643169720602
FDA Product Code
LWS, NVZ
EMDN Code
J01050101 Implantable single chamber defibrillators, with sensors
GMDN Term
Single-chamber implantable defibrillator
Device Class
Class AIMDD EUDAMED
Class III GUDID
EU market of registration
Netherlands
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Conditional

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00763000206208
00643169649347
00643169314207
00643169720602
GUDID
00643169720589
Device ClassEUDAMED
Class AIMDD
GUDID
Class III

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number

Other properties (19)

  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No