BEUDAMED
    13 results · 18ms · 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.

    PENTAX FD-34A DUODENOFIBERSCOPE

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

    DD cube ONE ML

    FDA UDI
    Dental Direkt GmbH·EDDIG8320061·DD cube ONE® ML are dental mill blanks made fro...

    VQ ORTHOCARE

    FDA UDI
    Vision Quest Industries Incorporated·00817717020548·OACTIVE2 OTS KO L HD, PUSH BUTTON

    VQ ORTHOCARE

    FDA UDI
    Vision Quest Industries Incorporated·00817717020531·OACTIVE2 OTS KO L, PUSH BUTTON

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024153561·

    Continuum® Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024153554·

    STERILE NITRILE POWDER FREE EXAMINATION GLOVE(VBLU), STERLE NITRILE POWDER FREE EXAMINATION GLOVE(ABLU)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LEGACY® IPC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KARL STORZ

    FDA Adverse Event
    Injury ·KARL STORZ ENDOSCOPY·Product code KQT·January 21, 2004

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 7, 2014

    MEGASUTURECUT NEEDLE DRIVER

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·November 14, 2012

    COBAS INTEGRA 800

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·September 13, 2010

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021