ClaripulseClaripulse™
Get Early Access
Back to Cardiac Rhythm Management

Ilivia 7 HF-T QP DF4 IS4 ProMRI Adverse Events: FDA MAUDE Data

BIOTRONIK SE & Co. KG · CRT-Defibrillator (CRT-D)

Total Reports

130

Reports (30d)

0

Active Signals

0

Open Recalls

0

Monthly Report Volume
Event Type Breakdown

Keep exploring

Related devices in CRM

CAPSUREFIX Novus

MEDTRONIC, INC. · 46,089 reports

→

EMBLEM S-ICD

BOSTON SCIENTIFIC CORPORATION · 38,723 reports

→

Sprint Quattro Secure S MRI SureScan

MEDTRONIC, INC. · 38,006 reports

→

CapSureFix Novus MRI SureScan

MEDTRONIC, INC. · 29,057 reports

→

Durata

ABBOTT (ST. JUDE MEDICAL) · 20,299 reports

→

Quadra Assura MP

ABBOTT (ST. JUDE MEDICAL) · 10,625 reports

→

Want automated safety signal detection?

Claripulse monitors these devices weekly and detects anomalies using 6 statistical methods — spike, trend, changepoint, peer-outlier, and more.

Get Early Access

Understanding this data

What FDA MAUDE data does and does not tell you

How these reports are filed, why raw counts mislead, and the limits to know before drawing conclusions.

→

How a safety signal is detected

What the "Active Signals" count above means and the methods that separate a real signal from noise.

→
Disclaimer: This system analyzes publicly available FDA MAUDE data. It does NOT provide medical advice. MAUDE data is de-identified. Do not attempt re-identification. Report counts may differ from the FDA's MAUDE search due to processing cadence and deduplication. Data is updated weekly.