4,218 results · 30ms · 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.

MCGHAN

FDA Adverse Event
Injury ·MCGHAN·Product code FTR·July 25, 2000

PHARMCHEK SWAET PATCH

FDA Adverse Event
Injury ·PHARMCHEM, INC.·Product code FMH·August 26, 2025

IMPELLA RP FLEX

FDA Adverse Event
Injury ·ABIOMED, INC.·Product code PYX·March 31, 2025

BIOZORB

FDA Adverse Event
Injury ·HOLOGIC, INC·Product code NEU·September 5, 2023

ACCESS HIGH SENSITIVITY TROPONIN I REAGENT

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code MMI·December 20, 2023

PLASMAX PLUS PLASMA CONCENTRATOR W/GPS III PLASMA CONCENTRATOR TUBE W/30ML ACD-A

FDA Adverse Event
Injury ·BIOMET BIOLOGICS·Product code LOQ·June 3, 2010

COULTER LH 500 ANALYZER

FDA Adverse Event
Injury ·BECKMAN COULTER INC.·Product code LOQ·December 1, 2010

COUMATRAK PROTIME TEST SYSTEM

FDA Adverse Event
Injury ·BOEHRINGER MANNHEIM CORPORATION-FREEMONT·Product code LOQ·February 13, 1995

COUMATRAK PROTIME TEST SYSTEM

FDA Adverse Event
Injury ·BOEHRINGER MANNHEIM CORPORATION-FREEMONT·Product code LOQ·February 9, 1995

COUMATRAK PROTIME TEST SYSTEM

FDA Adverse Event
Injury ·BOEHRINGER MANNHIEM CORPORATION-FREEMONT·Product code LOQ·October 12, 1994

COUMATRAK PROTIME TEST SYSTEM

FDA Adverse Event
Injury ·BOEHRINGER MANNHEIM CORPORATOOON-FREEMONT·Product code LOQ·December 23, 1994

BROTHER PRINTER

FDA Adverse Event
Injury ·ROCHE DIAGNOSTICS·Product code LOQ·December 20, 2002

RENU WITH MOISTURE LOC

FDA Adverse Event
Injury ·BAUSCH AND LOMB WITH MOISTURE LOC·Product code LPN·June 25, 2006

BAUSCH & LOMB MOISTURE LOC

FDA Adverse Event
Injury ·BAUSCH & LOMB RENU MOISTURE LOC·Product code LPN·May 19, 2007

TECNIS SYMFONY

FDA Adverse Event
Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·November 26, 2019

TECNIS SYMFONY

FDA Adverse Event
Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·November 22, 2019

PENTAX

FDA Adverse Event
Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·October 6, 2016

DIVERTICULOSCOPE - WEERDA

FDA Adverse Event
Injury ·KARL STORZ GMBH & CO. KG TUTTLINGEN, GERMANY·Product code EOQ·October 19, 2016

CLINITRON AT*HOME

FDA Adverse Event
Injury ·HILL-ROM BATESVILLE·Product code IOQ·December 9, 2016

EVIS EXERAII BRONCHOVIDEOSCOPE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·November 3, 2016