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

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PARCUS GRAFT FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CoRoent

FDA UDI
Nuvasive, Inc.·00887517596970·CoRoent Large MP Ti, 9x9x23mm 8°

KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392E

FDA 510(k)
FDA Class 2 ·Cardiovascular

BACT/ALERT PF CULTURE BOTTLE

FDA 510(k)
FDA Class 1 ·Microbiology

WAVEWRITER ALPHA 16

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 15, 2024

GEENEN PANCREATIC STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FGE·January 10, 2019

ROD, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

ILIAC SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019

OT VERIO TEST STRIPS

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 2, 2013

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code MDS·May 2, 2011

MICRO-DRIVER RX

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MAF·August 1, 2008

POLARIS SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020

GEENEN PANCREATIC STENT

FDA Adverse Event
Injury ·COOK ENDOSCOPY·Product code FGE·September 14, 2018

GEENEN PANCREATIC STENT

FDA Adverse Event
Injury ·COOK ENDOSCOPY·Product code FGE·September 14, 2018

GEENEN PANCREATIC STENT

FDA Adverse Event
Injury ·COOK ENDOSCOPY·Product code FGE·September 14, 2018

UNKNOWN

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·June 9, 2021

ZIMMON PANCREATIC STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·October 16, 2020

POLARIS TRANSLATION SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019