36 results · 29ms · Sources: EU EUDAMED, 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