24 results · 23ms · Sources: EU EUDAMED, US FDA

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PNEUMO PULSSOR III

FDA 510(k)
FDA Class 2 ·Anesthesiology

STRADIS

FDA UDI
STRADIS MEDICAL, LLC·M75268215701·CUSTOM SURGICAL KIT VEIN PACK

AURIGA QI

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

HNC-127-TRIO NEUROVASCULAR ARRAY COIL

FDA 510(k)
FDA Class 2 ·Radiology

SEVEN CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·May 20, 2014

UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·November 6, 2012

MP30 INTELLIVUE PATIENT MONITOR

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·August 27, 2010

ARCOS 19X190MM SPL TPR DIST

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 14, 2018

TI LOW PROFILE SCREW 6.5X50MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

TI LOW PROFILE SCREW 6.5X50MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

TI LOW PROFILE SCREW 6.5X70MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

FREEDOM CONSTR HD 36MM T1 +9MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWZ·March 13, 2018

ARCOS 19X190MM SPL TPR DIST

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

TI LOW PROFILE SCREW 6.5X40MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

TI LOW PROFILE SCREW 6.5X60MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

TI LOW PROFILE SCREW 6.5X30MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

PECK RT TFLANGE SZ24

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·March 13, 2018

TI LOW PROFILE SCREW 6.5X35MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

TI LOW PROFILE SCREW 6.5X35MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018

TI LOW PROFILE SCREW 6.5X30MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018