177 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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EXCIA TOTAL HIP SYSTEM 12/14 TRUNNION WITH CERAMIC HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
BIOLOX PROSTHESIS HEAD 12/14 28MM S
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code LWJ·April 14, 2014
BIOLOX PROSTHESIS HEAD 12/14 28MM S
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496060918·POWER UNISEX, SIZE M, FUCSIA FLUO, ANATOMIC COM...
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70609181·Mini Sprint-Brackets Roth .018" 200 Brackets 3 ...
ELASTYFREE SYNTHETIC POWDER-FREE SURGICAL GLOVE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM
FDA 510(k)
FDA Class 3
·Cardiovascular
BD PHOENIX PMIC110
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 19, 2021
BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·August 23, 2021
BD PHOENIX PANEL PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023
BD PHOENIX PANEL PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023
BD PHOENIX¿ PMIC/ID-106
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025
BD PHOENIX¿ PMIC/ID-106
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025
BD PHOENIX¿ PMIC/ID-106
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·April 15, 2024
BD PHOENIX¿ PMIC/ID-106
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 23, 2024
BD PHOENIX¿ PMIC/ID-106
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024
BD PHOENIX¿ PMIC/ID-106
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·April 16, 2013
GREENLIGHT ADDSTAT
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·March 14, 2011
SELOX ST 60
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code DTB·June 13, 2008