10 results
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72ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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CO-FLEX
FDA Adverse Event
Injury
·ANDOVER HEALTHCARE, INC.·Product code FRO·May 18, 2011
COFLEX NL
FDA Adverse Event
Injury
·ANDOVER HEALTHCARE INC.·Product code FQM·June 24, 2019
HIP PACK
FDA Adverse Event
Injury
·ANDOVER HEALTHCARE INC·Product code OJH·February 5, 2018
POWER FLEX MED/SELF-ADHERING ELASTIC BANDAGE
FDA Adverse Event
Malfunction
·ANDOVER HEALTHCARE, INC.·Product code FQM·June 2, 2016
CO-FLEX
FDA Adverse Event
Injury
·ANDOVER HEALTHCARE INC.·Product code FQM·June 17, 2016
COFLEX LF BANDAGE 1" STERILE
FDA Adverse Event
Malfunction
·ANDOVER HEALTHCARE INC. (A MILLIKEN HEALTHCARE LOC·Product code FQM·August 20, 2025
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 20, 2015
PROGAV 2.0 SYS PED.W/SA20 A.PRECHAMBER
FDA Adverse Event
Malfunction
·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·August 24, 2018
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·December 19, 2018
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 8, 2020