2,730 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VALIANT STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·January 29, 2020
VALIANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·January 29, 2020
V MUELLER BE 2847
FDA Adverse Event
Other
·ALLEGIANCE HEALTHCARE CORP.·Product code KAK·April 4, 2000
JAKO LARYNGEAL PROBE, ANGLED
FDA Adverse Event
Malfunction
·Product code KAK·April 28, 2000
STORZ
FDA Adverse Event
Injury
·STORZ·Product code KAK·August 11, 2023
ENLO FLO SUCTION IRRIGATOR PROBE
FDA Adverse Event
Malfunction
·DAVOL, INC.·Product code KAK·August 11, 1994
MAXILLARY OSTIOUM SEEKER PROBE
FDA Adverse Event
Malfunction
·EXPLORENT CHIRURGISCHE INSTRUMENTE GMBH·Product code KAK·May 17, 2017
PILLING WECK
FDA Adverse Event
Malfunction
·PILLING WECK SURGICAL SURGICAL DIVISION·Product code KAK·November 19, 1998
STORZ
FDA Adverse Event
Other
·STORZ INSTRUMENT CO·Product code KAK·February 10, 1999
Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperature
FDA Recall
Terminated
·Vital Signs Colorado Inc.·Product code KAK·August 17, 2012
Probe, Ent
FDA classification
FDA Class 1
·Probe, Ent
AMII AMERICA KIT
FDA UDI
InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)·08809986680235·
Endo Access
FDA UDI
TULSA DENTAL PRODUCTS LLC·D716EAK1·Endo Access Kit - Holder & Ins
MARCHON JAPAN K.K.
FDA registration
MARCHON JAPAN K.K.·3 products·🇯🇵 Japan
KOBAYASHI SHOJI K.K.
FDA registration
KOBAYASHI SHOJI K.K.·5 products·🇯🇵 Japan
Cardinal Health K.K.
FDA registration
Cardinal Health K.K.·10 products·🇯🇵 Japan
KATO KOGEI,K.K
FDA registration
KATO KOGEI,K.K·2 products·🇯🇵 Japan
INFELD OPTICA K.K
FDA registration
INFELD OPTICA K.K·2 products·🇯🇵 Japan
HOSHIDEN WAKAYAMA K.K.
FDA registration
HOSHIDEN WAKAYAMA K.K.·1 product·🇯🇵 Japan
BAK®
FDA UDI
ZIMMER SPINE, INC.·00889024333192·