312 results · 23ms · Sources: EU EUDAMED, US FDA

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PICCOLO COMPOSITE NAILING SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Xenon Rebreathing System

FDA UDI
BIODEX MEDICAL SYSTEMS, INC.·00718175005101·KIT, XENON CONVENIENCE, MOUTHPIECE AND ADMINIST...

RENOVA INTERNAL HEX IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

VACUETTE QUICKSHIELD WITH SNAPPY TUDE HOLDER

FDA 510(k)
FDA Class 2 ·General Hospital

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·May 29, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 17, 2011

MEDTRONIC SPRINT FIDELIS ICD LEAD

FDA Adverse Event
Injury ·MEDTRONIC·Product code LWS·August 21, 2008

ACCESS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·May 20, 2015

NMIC-312

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026

PANEL PHOENIX NMIC-312

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026

NI

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 29, 2016

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

NI

FDA Adverse Event
Malfunction ·NI·Product code FPA·March 8, 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

NI

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 24, 2016