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

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MODUILAR UNIPOLAR

FDA 510(k)
FDA Class 2 ·Orthopedic

HEARTWAY Power Mobility Scooter

FDA 510(k)
FDA Class 2 ·Physical Medicine

CONFLUENT SURGICAL MICROMYST APPLICATOR AND AIR PUMP, MODELS 20-5000, AP-A-6063

FDA 510(k)
FDA Class 2 ·General Hospital

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

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM INC.·Product code MDS·February 8, 2013

FLEXTEND

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVN·January 6, 2011

MINICAP

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·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