8 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACUFEX ENDOBUTTON PACK
FDA 510(k)
FDA Class 2
·Orthopedic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122765·K-WIRE - SINGLE TROCAR THREADED 1.8mm DIA x 230mm
SISTEMA DE IMPLANTE NACIONAL (S.I.N.); DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Synapse Cardiovascular
FDA 510(k)
FDA Class 2
·Radiology
URETEROSCOPE, 8,6/9,8 FR. X 430 MM, 7°, 6,4 FR. CHANNEL, WITH A0396
FDA Adverse Event
Injury
·OLYMPUS WINTER & IBE GMBH·Product code FGB·December 16, 2016
PROTECTA XT CRT-D
FDA Adverse Event
Injury
·IPG MFG SWITZERLAND·Product code LWS·February 9, 2013
PUMP MMT-522LNAB PRDGM INS BL EN ML
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·December 28, 2010
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·July 23, 2014