ECG analysis platform

EU MDR REGULATORY CONTENT PLACEHOLDER. EU MDR wording and eIFU placeholders - not approved for clinical use.

Cardiovolt ECG analysis

Sign in to access the Cardiovolt ECG analysis platform.

Device label

Medical device

Cardiovolt AIRE

Manufacturer

Cardiovolt.ai Ltd
86-90 Paul Street
London EC2A 4NE
United Kingdom

EC REP

Casus Europe B.V. [EN]
Lange Viestraat, 2b, 3511 BK
Utrecht

Software identification

Version 0.0.1-EU
Release date Not Approved

Instructions for Use

Consult Electronic Instructions for Use (IFU) https://ifu.example.invalid

EU MDR eIFU - PLACEHOLDER

Consult IFU for symbols glossary.

A paper IFU can be requested by emailing: support@cardiovolt.ai

A paper IFU will be made available at no additional cost within 7 days.

Unique Device Identification
PLACEHOLDER: (01)5070004854201(11)Not Approved(8012)0.0.1-EU
CE mark 3022