22 results · 34ms · Sources: EU EUDAMED, 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