9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DETACHABLE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODE
FDA 510(k)
FDA Class 2
·Physical Medicine
Malibu
FDA UDI
Seaspine Orthopedics Corporation·10889981081324·Tap, Short 5.0mm (for 5.5mm SCREW)
DURA BLUE STERILIZATION WRAP
FDA 510(k)
FDA Class 2
·General Hospital
SOLOGARD LOCKING PLUS SYRINGE WITH NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
MICROSTAAR INJECTOR CARTRIDGE
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code KYB·November 24, 2010
ENDURANT ABDOMINAL STENT GRAFT SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·January 11, 2013
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·July 3, 2014
smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·March 27, 2024
paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·October 2, 2024