DFM100 PMCF Registry

• Research type

  Research Study

• Full title

  Post Market Clinical Follow-Up Event Registry Study for Efficia DFM100 Defibrillator/Monitor

• IRAS ID

  359877

• Contact name

  Will Sabol

• Contact email

  will.sabol@philips.com

• Sponsor organisation

  Philips

• Duration of Study in the UK

  10 years, 2 months, 1 days

• Research summary

  This is an Open-label, Multi-center, Observational, Prospective Post-market Clinical Follow-up study. The objective of this PMCF Event Registry Study is to obtain device data from clinical sites to confirm the safety and performance of the Philips Efficia DFM100 defibrillator/monitor, and system components.

• REC name

  North of Scotland Research Ethics Committee 1

• REC reference

  25/NS/0108

• Date of REC Opinion

  30 Sep 2025

• REC opinion

  Favourable Opinion