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6719

by Medtronic, Inc. 2 variants

Ref 6719

6719 is a device classified as Active implantable (AIMDD) (EU), Class III (US) made by Medtronic, Inc., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-00763000059385) and listed in FDA GUDID since 22 Dec 2018 (UDI-DI 00763000059385), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE AIMDD

Valid until

No date given

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

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/AIMDD EUDAMED NumberB-00763000059385 Basic UDI-DI 00763000059385UDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00763000059385 UDI-DI Date22 Dec 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00763000059385 registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI 00763000059385 listed 22 Dec 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00763000059385
  2. Registered EUDAMED B-00763000059385

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Generic name
Implantable pulse generator port plug
Device name
Tachy Accessories 6719
Model / reference
6719
Primary DI / UDI-DI
00763000059385
Basic UDI-DI
B-00763000059385
FDA product code
LWS, NVY
EMDN code
J010580 Implantable defibrillators - accessories
GMDN term
Implantable pulse generator port plug
Device class
Class AIMDD EUDAMED
Class III GUDID
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class AIMDD
GUDID
Class III

Device class is stated on each registry's own scale: Class AIMDD in the EU (EUDAMED), Class III in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Implantable pulse generator port plug

Similar devices in this category

Other devices filed under CARDIAC FUNCTIONALITY IMPLANTABLE DEVICES.

Other devices from Medtronic, Inc.

See all devices from Medtronic, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (20, all answered No)