350 results · 22ms · Sources: EU EUDAMED, US FDA

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LMT NOMAG IC 1,5

FDA 510(k)
FDA Class 2 ·General Hospital

Baltic Denture System BDLoad

FDA UDI
Merz Dental GmbH·D7091033565·Baltic Denture System BDLoad BDLoad ↓ Sm7 PLSEu...

CARDIAC DIAGNOSTIC SYSTEM, MODEL CH2000

FDA 510(k)
FDA Class 2 ·Cardiovascular

HEARTSTREAM FR2 AED, MODEL M3860A,M3861A

FDA 510(k)
FDA Class 3 ·Cardiovascular

ARTICULEZE M HEAD 36MM +5

FDA Adverse Event
Injury ·DEPUY INTL., LTD. 8010379·Product code JDI·April 3, 2013

TRUFILL DCS ORBIT MINI COMPLEX FILL

FDA Adverse Event
Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code HCG·March 30, 2011

4.0 CANN.CANC.BONE SCREW

FDA Adverse Event
Injury ·DEPUY ACE S.A. 'R.L.·Product code HWC·April 23, 2008

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

BD VACUTAINER® BLOOD ALCOHOL DETERMINATIONS SODIUM FLUORIDE TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·June 21, 2019

BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 29, 2017

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 20, 2026

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025

BD PHOENIX¿ NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025