30 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Medline ENFit Syringe
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017866·K-Wire, Double Ended, Trocar Point, Diameter Si...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017873·K-Wire, Double Ended, Trocar Point, Diameter 0....
DUTECK BODY COMPOSITION ANALYZER
FDA 510(k)
FDA Class 2
·Cardiovascular
SILJETR SYSTEM
FDA 510(k)
FDA Class 2
·Dental
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·June 6, 2018
RESERVOIR 3ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 10, 2013
GOBED II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·June 30, 2011
CENTRICITY RA1000
FDA Adverse Event
Malfunction
·GE HEALTHCARE INTEGRATED IT SOLUTIONS·Product code LLZ·September 1, 2008
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·November 20, 2018
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·December 11, 2018
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·August 17, 2020
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·May 16, 2019
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·April 4, 2018
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·June 15, 2021
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·June 17, 2022
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·April 22, 2024
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Malfunction
·COOK INC·Product code CBI·November 19, 2020
ARNDT ENDOBRONCHIAL BLOCKER SET
FDA Adverse Event
Injury
·COOK INC·Product code CBI·May 3, 2024
BD LUER-LOK¿ SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·July 22, 2022