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

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    ESENSOR CF GENOTYPING TESTM ESENSOR SYSTEM, ESENSOR CYSTIC FIBROSIS GENOTYPING TEST, ESENSOR INSTRUMENT, MODELS XT-8

    FDA 510(k)
    FDA Class 2 ·Immunology

    MOBILE INFANT WARMER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code FMT·November 9, 2010

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065715·INTRAORAL ELASTICS 4,5 oz 5/16" blue

    KLINIDRAPE SURGICAL GOWNS, NON-REINFORCED, BASIC PROTECTIONS AND STANDARD PROTECTION

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

    FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IMN) MODEL B

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 2, 2013

    UNKNOWN DEPUY ASR FEMORAL HEAD SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.-8010379·Product code KXA·September 15, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·April 26, 2011

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 4, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 4, 2019

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 4, 2019

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 4, 2019

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 4, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 4, 2019