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Master Study of the BIOMONITOR III and Incision and Insertion Tool (FIT OneStep)

Syncope Clinical Trial

Official title:
BIO|MASTER.BIOMONITOR III

Clinical Trial Summary

This study is a post-market clinical follow-up (PMCF) study to identify and evaluate residual risks associated with the use of the BIOMONITOR III and BIOMONITOR IIIm that are discovered or remain even after risk analysis, risk mitigation and successful conformity assessment. Furthermore, this study will also provide additional data as required by regulatory authorities outside of the CE-region.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04025710
Study type Interventional
Source Biotronik SE & Co. KG
Contact
Status Completed
Phase N/A
Start date October 17, 2019
Completion date April 6, 2022
View Details
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