13 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PROPELLER HEAD
FDA UDI
Biomet Orthopedics, LLC·00880304417038·
Spark Violet™ 538 anti-human CD45
FDA UDI
BIOLEGEND, INC.·00810034701978·URL: https://www.biolegend.com/en-us/products/s...
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668111048·INSTRUMENT CASE SMALL ALUMINUM
DARCO SMALL SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
BD Contoured Base Pen Needle
FDA 510(k)
FDA Class 2
·General Hospital
AUTOPULSE RESUSCITATION SYSTEM MODEL 100
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·January 25, 2013
ZOOM CRITICAL CARE BED
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV.·Product code FNL·January 13, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·August 5, 2014
PEN NDL 32G 4MM PRO 100 BOX 1200 US
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMI·July 30, 2021
BD NANO¿ 2ND GEN PEN NEEDLES 32G X 4MM (100 COUNT)
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·October 25, 2023
BD PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·February 23, 2021
STEALTHSTATION S7
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·March 8, 2021