17 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HYSTEROSCOPIC MYOMA SCREW
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
VERTE-STACK® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902379550·SPACER 8915412 12MM ADD ON LORDOTIC SM
ES/ULTRA DISPLAY AND PROCESSING STATION
FDA 510(k)
FDA Class 1
·Radiology
FLOXIN SUSCEPTIBILITY TEST DISKS
FDA 510(k)
FDA Class 2
·Microbiology
ABL800 FLEX
FDA Adverse Event
Malfunction
·RADIOMETER MEDICAL APS·Product code CHL·March 20, 2020
ABL800 FLEX
FDA Adverse Event
Malfunction
·RADIOMETER MEDICAL APS·Product code CHL·March 5, 2020
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·June 4, 2014
INRATIO2
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·January 9, 2013
PARADYM
FDA Adverse Event
Malfunction
·SORIN BIOMEDICA C.R.M., S.R.L.·Product code MRM·November 4, 2010
RADIFOCUS GLIDECATH
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 14, 2020
RADIFOCUS GLIDECATH
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 3, 2024
RADIFOCUS GLIDECATH
FDA Adverse Event
Injury
·Product code DQO·November 3, 2020
RADIFOCUS GLIDECATH
FDA Adverse Event
Injury
·Product code DQO·November 3, 2020
RADIFOCUS GLIDECATH
FDA Adverse Event
Injury
·Product code DQO·November 3, 2020
RADIFOCUS GLIDECATH
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQO·January 24, 2023
RADIFOCUS ANGIOGRAPHIC CATHETER
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQO·September 26, 2018
ABL800 FLEX
FDA Adverse Event
Malfunction
·RADIOMETER MEDICAL APS·Product code CHL·June 24, 2020