Zio XT recommended by NICE in the latest CVD impact report to detect cardiac arrhythmias.

Click here to see the full report

Regulatory Information

Regulatory information on iRhythm medical devices is described on this website.   This information is applicable to references made to Zio branded medical devices.  iRhythm Technologies, Inc. 699 8th Street, Suite 600 San Francisco, CA 94103, U.S.A. is the Legal Manufacturer[SH1] [JW2]  of the medical devices listed below.

Zio™ ECG monitors

United States

Zioä monitor ECG monitor

510(k) cleared

 

Zioä AT monitor ECG monitor

510(k) cleared

 

Zioä XT monitor ECG monitor

510(k) cleared

 

Europe & Switzerland

(Currently only available in Austria, Netherlands and Spain)

Zioä monitor ECG monitor

CE marked 2797

EC REP

Emergo Europe

Westervoortsedijk 60

6827 AT Arnhem

The Netherlands

 

CH REP

MedEnvoy Switzerland

Gotthardstrasse 28

6302 Zug

Switzerland

 

 

UK

Zioä XT monitor ECG monitor

UKCA marked 0086

UKRP

Emergo Consulting (UK) Limited

c/o Cr360 – UL International, Compass House, Vision Park Histon, Cambridge CB24 9BZ

United Kingdom

 

Japan

Zioä ECG recording and analysis system

Medical device approval number: 30600BZI00018000

Sales name: Zio ECG recording and analysis system

General name: Long-term electrocardiogram data recorder

DMAH

Micren Healthcare Co., Ltd.

19-1 Harakata-cho, Shinjuku-ku, Tokyo

Software as a Medical Device (SaMD)

United States

Zioä  ECG Utilization Software (ZEUS)

510(k) cleared

 

Europe & Switzerland

(Currently only available in Austria, Netherlands and Spain)

Zioä ECG Utilization Software (ZEUS)

CE marked 2797

              The conformity mark applies to the following components:

−         SFW0073 ECGDL Algorithm

−         SFW0037 ZEUS QA Tool

−         SFW0030 Clinical Web Service and ZEUS Report

−         SFW0075 Clinical Analysis Service

 

EC REP

Emergo Europe

Westervoortsedijk 60

6827 AT Arnhem

The Netherlands

CH REP

MedEnvoy Switzerland

Gotthardstrasse 28

6302 Zug

Switzerland

 

UK

Zioä  ECG Utilization Software (ZEUS)

UKCA marked 0086

UKRP

Emergo Consulting (UK) Limited

c/o Cr360 – UL International, Compass House, Vision Park Histon, Cambridge CB24 9BZ

United Kingdom

 

Japan

Zioä ECG recording and analysis system

Medical device approval number: 30600BZI00018000

Sales name: Zio ECG recording and analysis system

General name: Long-term electrocardiogram data recorder

DMAH

Micren Healthcare Co., Ltd.

19-1 Harakata-cho, Shinjuku-ku, Tokyo

WEB0231.01