13 results · 19ms · Sources: EU EUDAMED, US FDA

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MODIFICATION OF THE IBI-1100 STEERABLE ELECTROPHYSIOLOGY CATHETER SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

Octane Mechanical Thrombectomy System

FDA 510(k)
FDA Class 2 ·Cardiovascular

EVIS MD PLANTIUM BLUE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

CIRCUITGUARD CIRCUITGUARD HME

FDA Adverse Event
Other ·ARC MEDICAL INC., ANESTHESIA & RESPIRATORY CARE·Product code BYD·July 20, 2005

BD MULTI-CHECK CD4 LOW CONTROL

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 29, 2023

BD MULTI-CHECK¿

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·May 5, 2023

BD MULTI-CHECK¿

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 22, 2023

BD MULTI-CHECK¿

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 22, 2023

VERSACARE BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·January 25, 2013

CURLIN INFUSION 4000CMS IV PUMP

FDA Adverse Event
Injury ·MOOG MEDICAL DEVICES GROUP·Product code FRN·January 24, 2011

530G INSULIN PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·August 5, 2014

BD MULTI-CHECK¿

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 26, 2023

BD MULTI-CHECK CD4 LOW CONTROL

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 16, 2023