Skip to content

myLUX™

by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation United States EUDAMED

Ref 7259

EMDN J010280

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number01915060000000000000363N7 Basic UDI-DIDate1 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Patient procedure pack
Model / Reference
7259
Primary DI / UDI-DI
00802526623851
Basic UDI-DI
01915060000000000000363N7
EMDN Code
J010280 Implantable cardiac diagnostic devices - accessories
Device Class
Class III
Medical Purpose
To provide compatible devices/products to facilitate remote monitoring and aid in the management of a patient and their insertable cardiac monitor.

Manufacturer details

EUDAMED SRN
US-PR-000022138

Other devices from Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation

See all devices from Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation →

Properties & raw data

Show properties, registry sources and raw records
Other properties (1)
  • Sterile: No

Sources (1)

  • EUDAMED 51ecd5fa-aea8-452a-9dcb-7159dd13f095 61 fields · synced 24 Oct 2026