64 results · 31ms · Sources: EU EUDAMED, US FDA

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MEDI-SIS SYRINGE INFUSION SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

NA

FDA UDI
Smith & Nephew, Inc.·00885556008201·BONE CURETTE STRAIGHT 228.6MM X ...

HUMMER IV MICRODEBRIDER SYSTEM

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

HORIZONTAL-VERTICAL LUMBAR VALVE AND SPETZLER LUMBAR PERITONEAL SHUNT SYSTEMS

FDA 510(k)
FDA Class 2 ·Neurology

UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

FDA Adverse Event
Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022

GYNECARE MORCELLEX* TISSUE MORCELLATOR

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code HET·May 14, 2013

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·September 23, 2014

PINN MAR +4 10D 32IDX48OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·May 13, 2011

TL PEDICLE SCREW DIA. 6,5 LG 50

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 50

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 35

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code HWC·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 40

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 45

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 35

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 50

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 50

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 50

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 45

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

TL PEDICLE SCREW DIA. 6,5 LG 40

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

FINAL SCREWDRIVER SHAFT - II

FDA Adverse Event
Malfunction ·ZIMMER SPINE·Product code NKB·February 15, 2016