18 results · 31ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

PERFUSOR SPACE

FDA Adverse Event
Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·April 5, 2023

DORNIER DIODE LASER FIBER

FDA Adverse Event
Malfunction ·DORNIER MEDTECH LASER GMBH·Product code GEX·July 1, 2019

AXIOM MEDICAL, INC

FDA Adverse Event
Malfunction ·AXIOM MEDICAL, INC.·Product code KDQ·February 6, 1998

ATRAUM

FDA Adverse Event
Malfunction ·AXIOM MEDICAL INC.·Product code KDQ·November 11, 2008

ANGLE SILICONE CATHETER, 32 FR

FDA Adverse Event
Malfunction ·AXIOM MEDICAL, INC.·Product code KDQ·October 20, 1994

THORACIC SILICONE CATHETER 32 FR.

FDA Adverse Event
Malfunction ·AXIOM MEDICAL, INC.·Product code KDQ·September 3, 1998

THORACIC SILICONE CATHETER RIGHT ANGLE 32 FR

FDA Adverse Event
Malfunction ·AXIOM MEDICAL, INC.·Product code KDQ·September 3, 1998

AXIOM ATRAUM THORACIC CATHETER

FDA Adverse Event
Malfunction ·AXIOM MEDICAL, INC.·Product code GBS·October 22, 2021

AXIOM

FDA Adverse Event
Malfunction ·AXIOM MEDICAL INC·Product code GCY·November 18, 2005

CWV DRAIN

FDA Adverse Event
Malfunction ·AXIOM MEDICAL, INC.·Product code BYY·August 16, 1993

THORACIC CATHETER 36 FR RIGHT ANGLE SILICONE

FDA Adverse Event
Malfunction ·AXIOM MEDICAL INC.·Product code KDQ·August 8, 1995

ATRAUM AXIOM ANGLE SILICONE CATHETER 36 FRENCH STOP CLOT

FDA Adverse Event
Malfunction ·AXIOM MEDICAL INC.·Product code FEZ·July 28, 1992

THORACIC SILICONE CATHETER

FDA Adverse Event
Malfunction ·AXIOM MEDICAL, INC.·Product code GBX·June 22, 2018

LEEP PRECISION GENERATOR

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code HGI·October 15, 2018

QUANTUM2000 ELECTROSURG.

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code HGI·May 9, 2019

LEEP PRECISION GENERATOR

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code HGI·October 16, 2018

LEEP PRECISION GENERATOR

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code HGI·May 31, 2019

LEEP PRECISION INTG. SYS.

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code HGI·July 16, 2019