18 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APRO 70 Catheter and Alembic Aspiration Tubing
FDA 510(k)
FDA Class 2
·Cardiovascular
7" (18 CM) APPX 0.45 ML, PRESSURE INFUSION (400PSIG) EXT SET W/ MICROCLAVE® CLEA
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·January 31, 2024
Philips
FDA UDI
Sbo Hearing A/S·05714464032549·HEARLINK 5030 MNR T BL/DG DEMO
Cooley Renal Artery Clamp 23cm
FDA UDI
Geister Medizintechnik GmbH·04057034062746·Cooley Renal Artery Clamp 23cm
MATRx plus
FDA 510(k)
FDA Class 2
·Anesthesiology
Z5 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
INVACARE FLORIDA OPERATIONS·Product code CAW·November 6, 2014
VIBRANT SOUNDBRIDGE
FDA Adverse Event
Injury
·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·August 17, 2011
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·July 16, 2013
VITEK® REVEAL¿ SENSOR PANEL
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·June 23, 2025
VITEK® REVEAL¿ SENSOR PANEL
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·June 24, 2025
VITEK® REVEAL¿ SENSOR PANEL
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·June 23, 2025
VITEK® REVEAL¿ SENSOR PANEL
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·June 24, 2025
VITEK® REVEAL¿ SENSOR PANEL
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·June 24, 2025
ACCESS® ACCUTNI+3 REAGENT
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code MMI·October 14, 2013
ACCESS® ACCUTNI+3 REAGENT
FDA Adverse Event
Injury
·BECKMAN COULTER·Product code MMI·October 14, 2013
ACCESS® 2 IMMUNOASSAY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·October 4, 2013
ACCESS® 2 IMMUNOASSAY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·October 4, 2013