8,051 results · 50ms · Sources: EU EUDAMED, US FDA

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FDA UDI
Fehling Instruments GmbH & Co. KG·04058749022308·CERAMO ZENKER vessel hook 25 x 3 x 175 mm

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749022292·CERAMO ZENKER vessel hook 10 x 3 x 175 mm, 22°

NA

FDA UDI
Fehling Instruments GmbH & Co. KG·04058749022315·CERAMO defect retractor 3 x 5 x 175 mm

DOS

FDA UDI
Shanghai AnQing Medical Instrument Co., Ltd·06970034210352·The video processor is used with the Single Use...

VENTR. TUNNEL. PRESS. KIT

FDA Adverse Event
Malfunction ·INTEGRA NEUROSCIENCES·Product code HCA·December 20, 2007

BD PEGASUS¿ SAFETY CLOSED IV CATHETER SYSTEM

FDA Adverse Event
Malfunction ·BD (SUZHOU)·Product code FOZ·July 26, 2019

PENTAX

FDA Adverse Event
Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·June 26, 2021

VISERA ELITE VIDEO SYSTEM CENTER

FDA Adverse Event
Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code HET·September 19, 2023

SMARTSET GMV 40G US EO

FDA Adverse Event
Injury ·DEPUY CMW - 9610921·Product code MBB·November 15, 2021

SMARTSET GMV 40G US EO

FDA Adverse Event
Injury ·DEPUY CMW - 9610921·Product code MBB·November 15, 2021

SINGLE USE BIOPSY VALVE (STERILE)

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·December 7, 2018

ORAL APPLIANCE

FDA Adverse Event
Injury ·AMERICAN SLEEP ASSOCIATION·Product code LRK·November 2, 2014

3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL.

FDA Enforcement
Class II ·Terminated·3M Company - Health Care Business·May 4, 2016

VISERA ELITE XENON LIGHT SOURCE

FDA Adverse Event
Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code NWB·September 27, 2023

BD PYXIS¿ MEDSTATION¿ ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·November 4, 2025

GRASPING FORCEPS

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code PTS·January 10, 2018

3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL.

FDA Recall
Terminated ·3M Company Health Care Business 3m Center·Product code FLF·January 22, 2016

UNK

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HRS·June 5, 2025

SMARTSET MV 40G - EO

FDA Adverse Event
Injury ·DEPUY CMW 9610921·Product code LOD·December 7, 2015

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017