104 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CarboClear Navigated Instruments
FDA 510(k)
FDA Class 2
·Neurology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694032773·1.2mm Standard Visidisk
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306823862·Marina Delicate Mallet, With Nylon Caps, 218 gr...
Adler Instrument Company
FDA UDI
Adler, Inc.·00810123203802·Metz Scissor, Curved, Regular,
3-PORT RADIAL PLUS
FDA UDI
The Wells Johnson Company·B458201251000·Cannula, 3-Port Radial Plus, specify length, di...
SNIPER, MODEL OR-3872XX SERIES
FDA 510(k)
FDA Class 2
·Cardiovascular
ST/AR ST AND ARRHYTHMIA SOFTWARE, RELEASE E.I.
FDA 510(k)
FDA Class 2
·Cardiovascular
3150 MRI MONITORING SYSTEM
FDA Adverse Event
Malfunction
·INVIVO RESEARCH, INC.·Product code DRT·January 2, 2003
PROSIMA PELVIC FLOOR REPAIR UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·September 5, 2018
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 11, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 27, 2014
SROM 28MM +0 M HEAD
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JDI·July 2, 2013
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·March 15, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·March 15, 2022
CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·March 15, 2022