36 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Endoscope Sterilization Tray
FDA 510(k)
FDA Class 2
·General Hospital
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515023833·Ribbon Retractor, 1 3/4" (4.5 cm) wide, 10" (25...
FRESENIUS MODEL 2008T HEMODIALYSIS MACHINE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
POWDERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
FDA 510(k)
FDA Class 1
·General Hospital
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·February 1, 2022
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·February 4, 2022
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·February 1, 2022
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·April 4, 2022
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·March 9, 2022
ROSA RECON PLATFORM 220V
FDA Adverse Event
Malfunction
·ZIMMER CAS·Product code OLO·March 21, 2022
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 20, 2013
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 7, 2011
EXTRACTOR RX RETRIEVAL BALLOON
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code FGE·September 29, 2008
ROSA RECON PLATFORM 220V
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code OLO·November 8, 2021
ROSA KNEE PLATFORM GB PL G
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·January 13, 2022
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·January 10, 2022
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·April 6, 2022
ROSA RECON PLATFORM 220V
FDA Adverse Event
Injury
·ZIMMER CAS·Product code OLO·January 10, 2022
MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code KRD·April 28, 2021
RINGLOC BI-POLAR 28X51MM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·February 14, 2024