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

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MODULAR REPLACEMENT ELBOW SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

DRILL 1.5X105MM 22MM STP J-NT

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HBE·June 16, 2021

DRILL 1.5X105MM 22MM STP J-NT

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HBE·April 28, 2021

DRILL 1.5X105MM 22MM STP J-NT

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HBE·June 4, 2021

SIMPLICITY SOFT QD MICRO INFUSION SET

FDA 510(k)
FDA Class 2 ·General Hospital

PAFLUFOCON C AND E DAILY CONTACT LENS

FDA 510(k)
FDA Class 2 ·Ophthalmic

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

PANEL PHOENIX NMIC-312

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 23, 2026

PANEL PHOENIX NMIC-312

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

PANEL PHOENIX NMIC-312

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

PANEL PHOENIX NMIC-312

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

PANEL PHOENIX NMIC-312

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

PANEL PHOENIX NMIC-312

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

PANEL PHOENIX NMIC-312

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

PANEL PHOENIX NMIC-312

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

PANEL PHOENIX NMIC-312

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

AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - ANTERIOR

FDA Adverse Event
Injury ·BARD SHANNON LIMITED·Product code FTL·April 12, 2013

RESTORE ULTRA

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·March 25, 2011

INSYTE IV CATHETER

FDA Adverse Event
Other ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·June 18, 2008