14 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SteriCap Safety Needle; VitreJect Safety Needle
FDA 510(k)
FDA Class 2
·General Hospital
alésoir Ø8
FDA UDI
FOURNITURES HOSPITALIERES INDUSTRIE·03661489333439·
WONDFO RAPID STREP A TEST
FDA 510(k)
FDA Class 1
·Microbiology
TRILOGY RADIOTHERAPY DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
BD PHOENIX¿ NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 21, 2024
COAGUCHEK ® XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·April 4, 2016
BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·December 28, 2018
BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·January 21, 2019
TAUT
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code GBZ·November 5, 2008
REFLECTION
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC·Product code JDH·September 2, 2011
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2013
INTIMA-II Y 24GAX0.75IN PRN/EC SLM
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·July 17, 2019
BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·December 18, 2019
ADVIA CENTAUR XP TESTOSTERONE (TSTO)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code CDZ·July 22, 2013