10,000 results · 74ms · Sources: EU EUDAMED, US FDA

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QFR SOLUTIONS BV

FDA registration
QFR SOLUTIONS BV·2 products·🇳🇱 Netherlands

QFR (3.0)

FDA 510(k)
FDA Class 2 ·Radiology

SYNERGY

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·May 13, 2026

ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·April 30, 2026

ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

FDA Adverse Event
Death ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·April 30, 2026

RESOLUTE INTEGRITY RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·July 10, 2020

XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Death ·ABBOTT VASCULAR·Product code NIQ·September 4, 2025

XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code NIQ·September 4, 2025

XIENCE XPEDITION

FDA Adverse Event
Injury ·ABBOTT VASCULAR INC.·Product code NIQ·March 2, 2026

XIENCE XPEDITION

FDA Adverse Event
Death ·ABBOTT VASCULAR INC.·Product code NIQ·March 2, 2026

Coagulation System For The Measurement Of Whole Blood Viscoelastic Properties

FDA classification
FDA Class 2 ·Coagulation System For The Measurement Of Whole Blood Viscoelastic Properties

XINCHANG PLASTIC HARDWARE MFR

FDA registration
XINCHANG PLASTIC HARDWARE MFR·1 product·🇨🇳 China

Percussionaire

FDA UDI
PERCUSSIONAIRE CORPORATION·00849436000228·Sinusoidal Bronchotron French

Omni 5 Fr. Seal Cap

FDA UDI
Hologic, Inc.·15420045513839·The Omni™ 5 Fr. Seal Caps are an accessory to t...

Percussionaire

FDA UDI
PERCUSSIONAIRE CORPORATION·00849436000471·Sinusoidal Bronchotron and Universal Monitron T...

Percussionaire

FDA UDI
PERCUSSIONAIRE CORPORATION·00849436000198·VDR4 - French

FR TECH, LLC

FDA registration
FR TECH, LLC·2 products·🇺🇸 United States

PULSE GUARD 3FR ELECTRODE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

2 FR KELMAN CHAMBER MAINTAINER

FDA 510(k)
FDA Class 2 ·General Hospital

VYGON 2 FR EPICUTANEO PUR-CATHETER

FDA 510(k)
FDA Class 2 ·General Hospital