FAQ

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What is the regulatory status of ECG Buddy in global markets?
ARPI's products are approved or registered for clinical use only in jurisdictions where the applicable regulatory requirements have been satisfied. Regulatory status may vary by country and is subject to change.  Please contact ARPI for the most current information regarding product availability and intended use in your region. Detailed information on regulatory approvals and registrations by market is provided below.European Union (EU)<ul><li>CE Marking under EU MDR (Regulation (EU) 2017/745) — Notified Body: BSI (NB 2797) </li><li>Classification: Class IIa</li></ul><hr>Taiwan <ul><li>TFDA (Taiwan Food and Drug Administration) - Medical Device License </li><li>Classification: Class II</li></ul><hr>Vietnam <ul><li>MOH (Ministry of Health) - Medical Device Registration</li><li>Classification: Class B</li></ul><hr>New Zealand <ul><li>Medsafe - WAND Notification </li><li>Classification: Class I</li></ul><hr>Australia <ul><li>ECG Buddy is entered in the ARTG, (ARTG number: 527556)</li><li>Classification: Class IIb </li></ul><hr>Please note, clinical use is permitted only in markets where the product has received the necessary regulatory approval or registration. In countries or regions where regulatory approval has not been obtained, EB Research is intended exclusively for research and educational purposes and is not intended for clinical diagnosis or patient management.
Published: 2026-06-19Read more
How can I delete my account?
You can deactivate your account by following the steps below. Your account will remain deactivated for 1 year and will then be automatically deleted.1. Log in to the ECG Buddy application. 2. Tap the 'Settings' icon. 3. Tap 'Delete Account'. 4. Tap “I have read, understood, and agree” to confirm account deletion.If you would like your account to be deleted immediately, please email us at <a href="mailto:[email protected]">[email protected]</a>.  
Published: 2026-02-01Read more

What is the regulatory status of ECG Buddy in global markets?

Published: 2026-06-19

ARPI's products are approved or registered for clinical use only in jurisdictions where the applicable regulatory requirements have been satisfied. Regulatory status may vary by country and is subject to change.  Please contact ARPI for the most current information regarding product availability and intended use in your region. Detailed information on regulatory approvals and registrations by market is provided below.European Union (EU)<ul><li>CE Marking under EU MDR (Regulation (EU) 2017/745) — Notified Body: BSI (NB 2797) </li><li>Classification: Class IIa</li></ul><hr>Taiwan <ul><li>TFDA (Taiwan Food and Drug Administration) - Medical Device License </li><li>Classification: Class II</li></ul><hr>Vietnam <ul><li>MOH (Ministry of Health) - Medical Device Registration</li><li>Classification: Class B</li></ul><hr>New Zealand <ul><li>Medsafe - WAND Notification </li><li>Classification: Class I</li></ul><hr>Australia <ul><li>ECG Buddy is entered in the ARTG, (ARTG number: 527556)</li><li>Classification: Class IIb </li></ul><hr>Please note, clinical use is permitted only in markets where the product has received the necessary regulatory approval or registration. In countries or regions where regulatory approval has not been obtained, EB Research is intended exclusively for research and educational purposes and is not intended for clinical diagnosis or patient management.