30 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MICHELANGELO BUNION SYSTEM - MABS, MODEL: MA6000
FDA 510(k)
FDA Class 2
·Orthopedic
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450584927·
OMNIDOS
FDA 510(k)
FDA Class 2
·Radiology
CRIT-LINE MONITOR III (CLM III)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
VASOVIEW 6 ACCESSORY PACK
FDA Adverse Event
Malfunction
·MAQUET CV·Product code GCJ·January 10, 2019
VASOVIEW 6 ACCESSORY PACK
FDA Adverse Event
Malfunction
·MAQUET CV·Product code GCJ·January 10, 2019
VASOVIEW 6 ACCESSORY PACK
FDA Adverse Event
Malfunction
·MAQUET CV·Product code GCJ·January 10, 2019
V SERIES MONITOR
FDA Adverse Event
Malfunction
·MINDRAY DS USA, INC.·Product code MHX·April 30, 2013
OVATIO
FDA Adverse Event
Injury
·SORIN CRM S.A.S.·Product code MRM·May 17, 2011
EBI OSTEOGEN IMPLANTABLE GROWTH STIMULATOR
FDA Adverse Event
Malfunction
·EBI, L.P.·Product code LOE·August 5, 2008
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·September 25, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·September 26, 2018
UPJ OCCLUSION BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZN·April 7, 2017
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·July 8, 2019
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·November 14, 2017
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·November 19, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·July 19, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·August 1, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·August 22, 2018
UNIVERSA SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code EZL·February 21, 2018