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