15 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Atellica IM Ferritin Assay
FDA 510(k)
FDA Class 2
·Immunology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293753·
MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ONCO TRAC MODEL 1, 2, 4
FDA 510(k)
FDA Class 2
·Radiology
3 ML BD SYRINGE WITH BD LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·March 12, 2018
BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM
FDA Adverse Event
Malfunction
·BD SUZHOU (MDS)·Product code FOZ·January 21, 2025
ACCU-CHEK ® MOBILE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 14, 2014
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·July 21, 2011
CORTSCR Ø1.5 SELF-TAP L6
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code MQN·June 15, 2013
3 ML BD LUER-LOK¿ DISPOSABLE SYRINGE WITH BD LUER-LOK¿ TIP
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 20, 2018
OPEN-END FLEXI-TIP URETERAL CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KOD·February 6, 2020
OPEN-END URETERAL CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KOD·February 7, 2020
BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM
FDA Adverse Event
Malfunction
·BD SUZHOU (MDS)·Product code FOZ·January 14, 2025
OPEN-END URETERAL CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KOD·December 5, 2019
Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)
FDA Enforcement
Class II
·Ongoing·Medtronic Inc.·November 29, 2017