22 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VIKINI Diode Laser System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HairCheck-DT (Cocaine)
FDA UDI
Quest Diagnostics·00868586000216·HairCheck-DT (Cocaine) is an ELISA test kit use...
MAKOPLASTY
FDA UDI
MAKO SURGICAL CORP.·00848486019846·Upper Tray THA Array Kit
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T1512320·15mm TLIF Implant 12mm Wide 32mm Length
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704283129·DEAVER RETRACTOR HOLLOW 1" X 12"
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587T15123270·15mm TLIF Implant 12mm Wide 32mm Length 7 Degrees
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869607735·TELIX K Ti Cage 12x32mm 5°
D731 MICRO 20 PH.I.S.I.O PEDIATRIC ARTERIAL FILTER, D733 MICRO 40 PH.I.SI.O PEDIATRIC ARTERIAL FILTER
FDA 510(k)
FDA Class 2
·Cardiovascular
JOINSOON ELECTRONICS MFG CO. LTD HIGH SPEED DIGITAL THERMOMETER, MODEL TC-001
FDA 510(k)
FDA Class 2
·General Hospital
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·June 20, 2017
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·August 1, 2017
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·July 25, 2017
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·August 17, 2017
RADIFOCUS OPTITORQUE
FDA Adverse Event
Malfunction
·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·March 21, 2017
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·October 8, 2014
DELTA SHUNT KIT, REGULAR, PERFORMANCE LEVEL 1
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROSURGERY·Product code JXG·June 21, 2011
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN·Product code CBK·June 26, 2017
OPTITORQUE ANGIOGRAPHIC CATHETER
FDA Adverse Event
Malfunction
·Product code DQO·January 20, 2021