9 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LILLIPUT 2 INFANT HOLLOW FIBER OXYGENATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
LILLIPUT 2
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·November 3, 2023
LANX SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SLM-1ER, SLM-2ER, SLM-3ER
FDA 510(k)
FDA Class 2
·Ophthalmic
ULTRATHANE COPE NEPHROURETEROSTOMY SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·July 9, 2021
TARGETING ARM T2 PROX. HUM.
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 27, 2012
DELTAPAQ - CERECYTE MICROCOIL
FDA Adverse Event
Malfunction
·MICRUS ENDOVASCULAR, LLC·Product code HCG·February 21, 2013
PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·January 27, 2011
TAPER SLEEVE ADAPTER 12/14 +8
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 31, 2014