294 results · 64ms · 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.

TERUMO MEDICAL CORP ANGIO-SEAL

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code MGB·March 25, 2026

OSFERION

FDA Adverse Event
Injury ·OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY·Product code MQV·March 19, 2020

FOUNDATION

FDA Adverse Event
Injury ·Product code LYC·March 19, 2020

PRECISE SDS SELF EXPANDING

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code FGE·July 2, 2014

PROTRACK MICROCATHETER

FDA Adverse Event
Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DQX·October 14, 2015

OSFERION

FDA Adverse Event
Injury ·OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY·Product code MQV·November 11, 2015

PINNACLE DESTINATION RENAL GUIDING SHEATH

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DYB·March 11, 2010

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DQX·February 5, 2010

TERUMO HEART LUNG MACHINE

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DTQ·April 28, 2014

PINNACLE DESTINATION CAROTID GUIDING SHEATH

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DYB·June 21, 2010

PINNACLE INTRODUCER SHEATH

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DYB·July 23, 1996

PINNACLE INTRODUCER SHEATH 8 FR

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DYB·July 30, 1996

PINNACLE INTRODUCER SHEATH

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DYB·August 16, 1996

GLIDEWIRE GUIDEWIRE .035/180

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DQX·September 10, 1996

SUREFLO INJECTION PLUG

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code FOZ·August 19, 1996

TERUMO PINNACLE INTRODUCER

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DYB·January 7, 2004

RADIFOCUS INTRODUCER II KIT

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP·Product code DYB·February 8, 2002

ARTIFICIAL KIDNEY

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code FJI·May 2, 1996

GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code DQX·June 7, 1996

ARTIFICIAL KIDNEY

FDA Adverse Event
Injury ·TERUMO MEDICAL CORP.·Product code FJI·May 2, 1996