12 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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U2 Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
Medline Industries, Inc.
FDA UDI
MEDLINE INDUSTRIES, INC.·10889942114870·MULTI 6X22" TYVEK PACK-LF
EVOLUTION MP TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CLEARVISION
FDA 510(k)
FDA Class 2
·Dental
COMPREHENSIVE REVERSE SHOULDER GLENOSPHERE MINI BASEPLATE WITH TAPER ADAPTER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·January 11, 2017
COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING / STANDARD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·January 11, 2017
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO INC·Product code GJS·June 5, 2013
HEARTSTART MRX -EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 19, 2014
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·June 17, 2011
ENDURANT STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·December 4, 2017
UNKNOWN
FDA Adverse Event
Injury
·COOK INC·Product code DYB·June 27, 2024
MICROPUNCTURE TRANSITIONLESS ACCESS SET
FDA Adverse Event
Injury
·COOK INC·Product code DYB·March 29, 2022