49 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEDROCEL VERTEBRAL BODY REPLACEMENT, MODEL XX-YYY-ZZZZ
FDA 510(k)
FDA Class 2
·Orthopedic
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890103780·Zirlux Titanium Abutment 6 mmH compatible with:...
Vivid Elegance Monophase RS
FDA UDI
PEARSON DENTAL SUPPLIES, INC.·D724D0103780·50ml x 4
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182444·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182475·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182451·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182499·
JOE FRESH
FDA UDI
FGX INTERNATIONAL INC.·00193033182482·
BIOCUFF, MODELS 225718, 225728, 225736, 235718, 235728, 235736
FDA 510(k)
FDA Class 2
·Orthopedic
BACT/ALERT MB CULTURE BOTTLE
FDA 510(k)
FDA Class 1
·Microbiology
CADD
FDA UDI
ICU MEDICAL, INC.·15019517096392·
NATUS BRAIN MONITOR BREAKOUT
FDA Adverse Event
Malfunction
·NATUS MEDICAL INCORPORATED·Product code GWQ·July 31, 2023
IP PTZ HD ERGOJUST VIDEO EXTENSION
FDA Adverse Event
Malfunction
·NATUS MEDICAL INCORPORATED·Product code GWQ·October 12, 2020
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC., USA·Product code LFR·May 11, 2007
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·March 19, 2013
SHUNT SENSOR SYS500
FDA Adverse Event
TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·February 24, 2011
MOBILE CART CAMERA
FDA Adverse Event
Malfunction
·NATUS MEDICAL INCORPORATED·Product code FTT·March 9, 2020
NATUS BRAIN MONITOR BREAKOUT
FDA Adverse Event
Malfunction
·NATUS MEDICAL INCORPORATED·Product code GWQ·July 31, 2023
TROLLEY CART
FDA Adverse Event
Malfunction
·NATUS MEDICAL INCORPORATED·Product code NYE·August 17, 2023
EMU40EX BASE UNIT
FDA Adverse Event
Malfunction
·NATUS MEDICAL INCORPORATED·Product code GWQ·October 29, 2020