26 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REVERE STABILIZATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450456064·
MONARCH SPINAL SYSTEMS
FDA 510(k)
FDA Class 2
·Orthopedic
BIOMET LATERAL TROCH PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
PS FEMORAL COMPONENT CLOSED BOX LGE RIGHT 74 MM CEMENTED
FDA Adverse Event
Malfunction
·BIOMET SPAIN, S.L.·Product code JWH·June 3, 2020
VELA VENTILATOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code CBK·July 21, 2015
VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 63/67 X 18MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·October 20, 2016
VG DA 360 O/S TIB TRAY COCR 63
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·June 2, 2016
VG DA360 TIB BRG ARCM 71/75X24
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 7, 2016
VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 79/83 X 14MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·December 6, 2016
VG DA 360 O/S TIB TRAY COCR 71
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·June 1, 2016
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 22, 2015
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - AIBONITO·Product code FRN·May 6, 2013
DERMABOND TOPICAL SKIN ADHESIVE
FDA Adverse Event
Injury
·ETHICON INC.·Product code MPN·September 16, 2014
VG DA 360 O/S TIB TRAY COCR 67
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code JWH·August 3, 2018
VANGUARD DA360 TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 14, 2017
VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 63/67 X 18MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·February 6, 2017
VELA VENTILATOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code CBK·February 19, 2015
VG DA 360 TIB BRG ARCM 79/83X14
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 19, 2016
BD CONNECTA PLUS3 WHITE PEGS
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·June 3, 2024