BEUDAMED
    13 results · 30ms · 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.

    BARD SINGULAR BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0142120·Trial, TLIF, 32L OB CRV 7Deg, 12mm

    HIGH-PRESSURE CONNECTOR TUBE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BARD CONQUEST PTA BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN DEPUY 52X28MM +4 LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·December 1, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code CAW·July 3, 2014

    T-PAL LARGE TRIAL IMPLANT SIZ 7 NON DETA

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HSB·December 7, 2012

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 30, 2013

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 30, 2013

    CORAIL2 STD SIZE 10

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWA·October 9, 2013

    AGILIA VP MC WIFI AU

    FDA Adverse Event
    Malfunction ·FRESENIUS VIAL S.A.S.·Product code FRN·November 26, 2024

    AGILIA VP MC WIFI AU

    FDA Adverse Event
    Malfunction ·FRESENIUS VIAL S.A.S.·Product code FRN·November 26, 2024

    Pipeline Flex Embolization Device

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