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

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CERAMAFLEX BRACKET SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

CONMED IRRIGATION NOZZLE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Vios Monitoring System

FDA 510(k)
FDA Class 2 ·Cardiovascular

S3 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR)·Product code DTQ·April 23, 2010

3 TO 1 REDUCTION DRIVE

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 14, 2011

S3 ROLLER PUMP MODULE AND CONSOLE

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR·Product code DTQ·March 24, 2010

3-TO-1 REDUCTION DRIVE

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHMAND·Product code DTQ·December 14, 2011

STOCKERT S3 CONSOLE

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·October 6, 2011

STOCKERT S3 CONSOLE

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·October 6, 2011

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·February 8, 2013

OMNIPOD INSULIN PUMP

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·January 3, 2011

NIM RESPONSE® 3.0 PATIENT INTERFACE

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·July 22, 2014

SENSOR, LOW LEVEL II

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 16, 2010

S3 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR)·Product code DTQ·April 23, 2010

S3 ROLLER PUMP

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 22, 2010

S3 ROLLER PUMP

FDA Adverse Event
SORIN GROUP DEUTSCHLAND·Product code DWB·October 12, 2016

BLOOD CARDIOPLEGIA INSERTS

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·March 24, 2010

INSET W. LUER-LOCK, 10PK, US, 6MM/23", GREY, INF SET

FDA Adverse Event
Injury ·UNOMEDICAL A/S·Product code FPA·November 8, 2024