28 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
AGILIS NXT STEERABLE INTRODUCER
FDA 510(k)
FDA Class 2
·Cardiovascular
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169601314·SPACER 2110450 OLIF25 20MM 0 DEG 14X50
Medtronic Reusable Instruments
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902096310·REAMER 9110450 ADJ 18MM TPRD
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074148526·SCREW 8110450 NA LP CROSSLINK SET TI
Humelock II Cemented Shoulder System
FDA UDI
FX SOLUTIONS·03701037306796·DRILL BIT Ø4.5mm L150mm/ AO
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K1103500·Tray, Base, 3.5", Arcamed
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100500·Caddie, 4.75mm Screws
I-ROOT
FDA 510(k)
FDA Unclassified
·Unknown
LIVER TAMPONADE BALLOON
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 13, 2013
GO BED PLUS
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·April 25, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 14, 2008
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 14, 2017
CANTATA 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·November 17, 2017
BD PEGASUS SAFETY CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·August 7, 2023
CANTATA 2.5 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 17, 2018
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·September 11, 2018
CANTATA 2.5 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·July 28, 2017
CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·June 15, 2017
CANTATA 2.5 SUPERSELECTIVE MICROCATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·May 30, 2018