BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    FIBERFLO HOLLOW FIBER CAPSULE WATER FILTERS

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

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983126·posteriors; shade D4; size S; upper jaw

    TIBIAL NAIL, STANDARD 10X390 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·March 17, 2010

    Electrosurgical accessory

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BREVET DENTAL INSTRUMENTS

    FDA 510(k)
    FDA Class 1 ·Dental

    TRIAGE PROFILER SOB PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·June 27, 2019

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 25, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 28, 2013

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 31, 2011

    Basic Pack, part number AMS1868(B Basic Pack, part number AMS2608(A Basic Pack, part number AMS3861 Basic Pack, part number AMS4309 Basic Pack, part number PSS1833 Basic Pack, part number PSS1833(A Basic Pack, part number PSS1848(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017