54 results · 39ms · Sources: EU EUDAMED, US FDA

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PHOENIX ISE STANDARD A,B AND C FOR ROCHE/AVL SYSTEMS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

PicoDriver

FDA UDI
LSI Solutions, Inc.·00850012846437·PicoDriver Device

ISAAC 1.5 T MR SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

Z-TOUCH

FDA 510(k)
FDA Class 2 ·Neurology

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION CORPORATION·Product code FRN·February 27, 2013

UNKNOWN ZIMMER NATURAL NAIL

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code HSB·February 15, 2011

IMPLANTIUM

FDA Adverse Event
Injury ·DENTIUM·Product code DZE·March 31, 2008

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQX·October 16, 2009

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 7, 2025

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 6, 2026

SYNCHRO GUIDEWIRE

FDA Adverse Event
Death ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·August 2, 2010