26 results · 24ms · Sources: EU EUDAMED, 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