BEUDAMED
    36 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Sulbactam-durlobactam in the dilution range of 0.015/4-32/4 ug/mL

    FDA 510(k)
    FDA Class 2 ·Microbiology

    LINVATEC 300W XENON LIGHT SOURCE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SOMNOLYZER 24X7

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DANEK SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code HWC·June 4, 1999

    CRYOVALVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MIE·June 24, 1998

    INNER SHEATH, FOR 26 FR. OUTER SHEATH

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·August 8, 2024

    REMANUFACTURED CENTURY STERILIZER

    FDA Adverse Event
    STERIS MEXICO, S. DE R.L. DE C.V.·Product code FLE·March 26, 2015

    RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR. OUTER SHEATH, ABS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·August 13, 2024

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 6, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·September 1, 2011

    DEROYAL SURGIMATE 35W 24/CASE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDT·July 15, 2013

    RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR. OUTER SHEATH, ABS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·April 25, 2024

    INNER SHEATH, FOR 26 FR. OUTER SHEATH

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·August 6, 2024

    INNER SHEATH, FOR 26 FR. OUTER SHEATH

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·November 7, 2024

    ALPHA I INFLATABLE PENILE PROSTHEIS

    FDA Adverse Event
    Injury ·MENTOR UROLOGY, INC.·Product code FHW·October 11, 1996

    RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR. OUTER SHEATH, ABS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·September 29, 2023

    RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR. OUTER SHEATH, ABS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·July 6, 2023

    RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR. OUTER SHEATH, ABS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·November 6, 2023

    RESECTION SHEATH, 26 FR.

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·November 6, 2023

    INNER SHEATH, FOR 26 FR. OUTER SHEATH

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·November 14, 2023