17 results · 27ms · Sources: EU EUDAMED, US FDA

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DENTAL DAM

FDA 510(k)
FDA Class 1 ·Dental

ADVANCE(R) PREGNANCY TEST

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

EMIT CONVENIENCE PACK, QUINIDINE ASSAY/CALIBRATORS

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

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

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·February 11, 2013

DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

PULSE GEN MODEL 105

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·July 24, 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