7,121 results · 33ms · Sources: EU EUDAMED, US FDA

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REUS,NK SPO2 SNSR,63",ADLT FNG CLP

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828187572·REUS,NK SPO2 SNSR,63",ADLT FNG CLP

REUS,NK SPO2 SNSR,39",PED FNG CLP

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828187602·REUS,NK SPO2 SNSR,39",PED FNG CLP

REUS,NK SPO2 SNSR,39",ADLT FNG CLP

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828187589·REUS,NK SPO2 SNSR,39",ADLT FNG CLP

REUS,NK SPO2 SNSR,63",PED FNG CLP

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828187596·REUS,NK SPO2 SNSR,63",PED FNG CLP

NON AC-POWERED PATIENT LIFT

FDA Adverse Event
Malfunction ·UNKNOWN·Product code FSA·November 8, 2013

KRAYENBUEHL HK FNG REST SML

FDA Adverse Event
Malfunction ·CARDINAL HEALTH·Product code GDG·October 8, 2003

EDM VENTRICULAR CATHETER, BARIUM IMPREGNATED, 35 CM

FDA Adverse Event
Injury ·MEDTRONIC NEUROSURGERY·Product code GWM·August 5, 2019

ENTROY

FDA Adverse Event
Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FNG·October 28, 2016

CLIP SLINGS

FDA Adverse Event
Malfunction ·MEDIBO MEDICAL PRODUCTS N.V.·Product code FNG·January 3, 2012

MEDCARE

FDA Adverse Event
Malfunction ·MEDCARE PRODUCTS·Product code FNG·February 21, 2012

VOYAGER

FDA Adverse Event
Malfunction ·ARJOHUNTLEIGH MAGOG·Product code FNG·March 2, 2012

VOYAGER

FDA Adverse Event
Malfunction ·ARJOHUNTLEIGH MAGOG, INC·Product code FNG·February 27, 2012

MAXI TWIN

FDA Adverse Event
Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FNG·March 20, 2012

HOYER PRESENCE LIFT WITH SCALE

FDA Adverse Event
Malfunction ·SR INSTRUMENTS·Product code FNG·March 27, 2012

MAXI SKY 600 CEILING LIFT

FDA Adverse Event
Malfunction ·ARJOHUNTLEIGH, INC·Product code FNG·January 13, 2012

VOYAGER

FDA Adverse Event
Injury ·ARJOHUNTLEIGH MAGOG·Product code FNG·February 24, 2012

MEDCARE

FDA Adverse Event
Other ·MEDCARE PRODUCTS·Product code FNG·February 15, 2012

HOYER HML-400 LIFT WITH HOYER SLING

FDA Adverse Event
Malfunction ·STARITE INTERNATIONAL, LTD.·Product code FNG·March 31, 2012

ERGOLIFT

FDA Adverse Event
Malfunction ·BHM MEDICAL, INC.·Product code FNG·February 8, 2009

8030916-2008-00058

FDA Adverse Event
Malfunction ·Product code FNG·January 28, 2009