44 results · 22ms · Sources: EU EUDAMED, US FDA

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MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS

FDA 510(k)
FDA Class 2 ·Anesthesiology

N/A

FDA UDI
BIOMET MICROFIXATION, INC·00841036011222·

BETSEY JOHNSON

FDA UDI
FGX INTERNATIONAL INC.·00193033541142·

BETSEY JOHNSON

FDA UDI
FGX INTERNATIONAL INC.·00193033541128·

BETSEY JOHNSON

FDA UDI
FGX INTERNATIONAL INC.·00193033541111·

BETSEY JOHNSON

FDA UDI
FGX INTERNATIONAL INC.·00193033541135·

Internal Handle

FDA UDI
Zoll Medical Corporation·00847946022365·

ACTI-ICP MONITORING SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

SNIPER ELITE MODEL-OR-E3872XX SERIES

FDA 510(k)
FDA Class 2 ·Cardiovascular

TRILOGY 200

FDA Adverse Event
Malfunction ·RESPIRONICS INC·Product code CBK·August 19, 2020

DIDECO LILIPUT ECMO M PHISIO

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·April 20, 2012

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
Malfunction ·UNKNOWN·Product code ITJ·March 20, 2013

TENDRIL ST

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011

GE OEC 9800

FDA Adverse Event
Malfunction ·Product code JAA·March 18, 2008

METASUL, ALPHA INSERT, II/32

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·March 15, 2018

METASUL, ALPHA INSERT, II/32

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code KWA·June 25, 2018

DURASUL, ALPHA INSERT, KK/36

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LZO·March 6, 2018

DURASUL, ALPHA INSERT, HOODED, MM/28

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code JDI·May 22, 2018

DURASUL, ALPHA INSERT, HH/32

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code LZO·June 4, 2018

DURASUL, ALPHA INSERT, HOODED, LL/32

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code JWH·April 23, 2018