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

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SenTec Digital Monitor, OxiVenT Sensor, V-Sign Sensor, Staysite Adhesive Pad, V-STATS PC Software including V-CareNet

FDA 510(k)
FDA Class 2 ·Anesthesiology

Flextrode

FDA UDI
COSMAN MEDICAL, LLC·08132500133826·Electrode 15cm, 13mm Tip, 20G

NA

FDA UDI
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·00813250013382·Flextrode, 15cm,17G Introducer

SYNERGY CT PICC

FDA 510(k)
FDA Class 2 ·General Hospital

STERILE POWDER-FREE LATEX EXAMINATION GLOVES WITH POLYMER COATING AND PROTEIN CLAIM (50 UG OR LESS)

FDA 510(k)
FDA Class 1 ·General Hospital

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code HAW·November 10, 2017

CONFIRM

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code MXC·January 13, 2014

DISTAL TARGETING DEVICE GAMMA3 DISTAL TARGETING R1.5

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·June 7, 2013

CLAVICLE PIN ASSEMBLY 2.5MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDW·June 30, 2011

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·April 11, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·March 15, 2018

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code HAW·June 15, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·November 10, 2017

LINEAR ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·January 2, 2025

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

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·March 21, 2018