Skip to content

6725

by Medtronic, Inc.

Ref 6725

6725 is a device classified as Active implantable (AIMDD) (EU), Class III (US) made by Medtronic, Inc., registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI B-00613994501646) and listed in FDA GUDID since 23 Sep 2014 (UDI-DI 00613994501646), 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-00613994501646 Basic UDI-DI 00613994501646UDI-DIDate4 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00613994501646 UDI-DI Date23 Sep 2014ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00613994501646 registered 4 Nov 2026 Active
  • FDA GUDID UDI-DI 00613994501646 listed 23 Sep 2014 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00613994501646
  2. Registered EUDAMED B-00613994501646

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  • Withdrawn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
Model 6725 Pin-Plug Kit
Model / reference
6725
Primary DI / UDI-DI
00613994501646 EUDAMED
00613994501035 GUDID
Basic UDI-DI
B-00613994501646
FDA product code
DXY, LWS, NAB
EMDN code
J010180 Implantable pacemakers - accessories
GMDN term
Implantable pulse generator port plug
Device class
Class AIMDD EUDAMED
Class III GUDID
Regulation number
870.3610, 878.4014
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
00613994501646
GUDID
00613994501035
Device classEUDAMED
Class AIMDD
GUDID
Class III

The registries describe this device under different primary UDI-DIs (EUDAMED lists 00613994501646; FDA GUDID lists 00613994501035), so their flags are not compared. 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 IMPLANTABLE PACEMAKERS.

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)