51 results · 27ms · Sources: EU EUDAMED, US FDA

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ISOFLOW INFUSION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014609874·MIDMARK 3" DELUXE

CAVITAT ULTRASOUND BONE DENSITOMETER (CAVITAT)

FDA 510(k)
FDA Class 2 ·Dental

ENHANCED POLYETHYLENE KNEE PROSTHESES

FDA 510(k)
FDA Class 2 ·Orthopedic

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 8, 2024

DUO FLUID CART

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·December 21, 2017

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·August 31, 2018

MUSTANG¿

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·April 26, 2013

SMARTSITE INFUSION SET

FDA Adverse Event
CAREFUSION·Product code FPA·April 27, 2011

PRISMA

FDA Adverse Event
Malfunction ·GAMBRO RENAL PRODUCTS, INC.·Product code FJK·July 11, 2008

ULTRAFLEX DUO HIGH FLUID CART - REFURBISHED

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·June 25, 2020

EVAC STATION

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·September 5, 2017

ULTRAFLEX DUO HIGH FLUID CART WITH SMOKE EVACUATOR

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·January 11, 2018

EVAC STATION

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·January 16, 2018

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·June 7, 2018

ULTRAFLEX DUO HIGH FLUID CART WITH SMOKE EVACUATOR

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·August 3, 2017

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·March 19, 2018

ULTRA DUO HIGH FLUID CART

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·December 27, 2017

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·October 9, 2018

ULTRA DUO HIGH FLUID CART NON-STERILE INSTRUCTIONS FOR USE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·February 12, 2018