22 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ONE-WAY VALVE (WITH CONNECTOR)
FDA 510(k)
FDA Class 2
·Anesthesiology
artegral
FDA UDI
Merz Dental GmbH·D7091970780·anteriors; shade B1; mould UBIM
F.A.S.T. 1
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·May 30, 2006
CONMED LINVATEC XO BUTTON
FDA 510(k)
FDA Class 2
·Orthopedic
ARIX Foot System (2.3/2.8)
FDA 510(k)
FDA Class 2
·Orthopedic
FASTI INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
FAST1 INTRAOSSEOUS INFUSION SYSTEM
FDA Adverse Event
Other
·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009
LC PCA III INFUSER
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code MEA·April 29, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·February 20, 2013
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·January 25, 2011
COMPREHENSIVE FIXED LOCKING SCREW 4.75MM X 15MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·April 20, 2017
COMPREHENSIVE REVERSE SHOULDER 6.5MM CENTRAL SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·April 20, 2017
COMPREHENSIVE FIXED LOCKING SCREW 4.75X30MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·April 20, 2017
COMPREHENSIVE SHOULDER SYSTEM PRIMARY STANDARD LENGTH SHOULDER STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·April 20, 2017
COMPREHENSIVE FIXED LOCKING SCREW 4.75X20MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·April 20, 2017