Skip to content

Livewire™ 401923

by St. Jude Medical Cardiovascular Division

Ref 401923

Livewire™ 401923 is a device classified as Class III in the EU and Class II in the US made by St. Jude Medical Cardiovascular Division, registered in EUDAMED on 31 Aug 2026 (Basic UDI-DI B-05414734202602) and listed in FDA GUDID since 6 Feb 2015 (UDI-DI 05414734202602), active as of 24 Oct 2026.

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

CE MDD

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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-05414734202602 Basic UDI-DI 05414734202602UDI-DIDate31 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05414734202602 UDI-DI Date6 Feb 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-05414734202602 registered 31 Aug 2026 Active
  • FDA GUDID UDI-DI 05414734202602 listed 6 Feb 2015 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05414734202602
  2. Registered EUDAMED B-05414734202602

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Livewire™
Generic name
Cardiac mapping catheter, percutaneous, single-use
Device name
Livewire Electrophysiology Catheter
Model / Ref / Catalog
401923
Primary DI / UDI-DI
05414734202602
Basic UDI-DI
B-05414734202602
FDA product code
DRA, DRF
EMDN code
C02010401 Arrhythmology multipolar diagnostic catheters, conventional
GMDN term
Cardiac mapping catheter, percutaneous, single-use
Device class
Class III EUDAMED
Class II GUDID
Regulation number
870.1280, 870.1220
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 6 French

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class III
GUDID
Class II

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

Related devices

Category: Cardiac mapping catheter, percutaneous, single-use

Similar devices in this category

Other devices filed under ARRHYTHMOLOGY MULTIPOLAR DIAGNOSTIC CATHETERS.

Other devices from St. Jude Medical Cardiovascular Division

See all devices from St. Jude Medical Cardiovascular Division →

Properties

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