258 results · 114ms · 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.

Sterilization Container Systems and Accessories

Basic UDI-DI
EU MDR · Eu Md Class 1 ·Victoris Health Tıbbi Cihazlar AŞ·939 devices

MARKERS

FDA Adverse Event
Malfunction ·PRAXIM·Product code HAW·January 3, 2007

INTEGRA RESERVOIR 1.5CM DOME, FLAT BOTTOM, SIDE

FDA Adverse Event
Malfunction ·INTEGRA NEUROSCIENCES PR·Product code JXG·June 5, 2017

VENACURE EVLT

FDA Adverse Event
Malfunction ·ANGIODYNAMICS, INC.·Product code GEX·March 14, 2024

HEARTMATE 3 LVAS MINI APICAL CUFF KIT

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·September 10, 2024

THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·September 10, 2024

THORATEC® HEARTMATE® GOGEAR®, SHOWER BAG

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·January 13, 2025

ARCTIC SUN® TEMPERATURE MANAGEMENT SYSTEM, FILL TUBE

FDA Adverse Event
Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·March 7, 2023

LIFESTENT 5F VASCULAR STENT SYSTEM

FDA Adverse Event
Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·November 29, 2018

EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·October 8, 2021

ENDOWRIST

FDA Adverse Event
Injury ·INTUITIVE SURGICAL, INC·Product code NAY·October 18, 2023

EVIS LUCERA GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·August 1, 2023

PUREWICK URINE COLLECTION SYSTEM

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code NZU·June 14, 2021

R15/BAG, DRAIN

FDA Adverse Event
Malfunction ·TIDI PRODUCTS LLC·Product code MMZ·October 1, 2025

EVIS EXERA III COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDF·August 11, 2021

ARCTIC SUN® 5000

FDA Adverse Event
Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·October 7, 2024

EVIS LUCERA ELITE COLONOVIDEOSCOPE

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDF·February 3, 2022

SOLERO

FDA Adverse Event
Malfunction ·ANGIODYNAMICS, INC.·Product code NEY·December 3, 2025

SOLERO

FDA Adverse Event
Malfunction ·ANGIODYNAMICS, INC.·Product code NEY·March 4, 2026

PEDIMAG BLOOD PUMP

FDA Adverse Event
Malfunction ·THORATEC SWITZERLAND GMBH·Product code QNR·June 12, 2024