BEUDAMED
    1,735 results · 26ms · Sources: EU EUDAMED, US FDA

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    KOOS MEDICAL INNOVATIONS Inc.

    FDA registration
    KOOS MEDICAL INNOVATIONS Inc.·1 product·🇺🇸 United States

    Koo (Shanghai) Industries Co., Ltd

    FDA registration
    Koo (Shanghai) Industries Co., Ltd·9 products·🇨🇳 China

    KOO SMALL VOLUME NEBULIZER (SVN)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KOO MEDICAL EQUIPMENT (SHANGHAI) CO. LTD.

    FDA registration
    KOO MEDICAL EQUIPMENT (SHANGHAI) CO. LTD.·2 products·🇨🇳 China

    KOO AMERICAS VALVE PEEP, MODEL KM-809

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UNKN PEEK INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·October 19, 2022

    UNK KNEE TIBIAL INSERT SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·September 14, 2022

    UNK KNEE FEMORAL SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 14, 2022

    HOUVA 4

    FDA Adverse Event
    Injury ·NATIONAL BIOLOGICAL CORP.·Product code KGL·May 28, 2015

    UNK KNEE TIBIAL TRAY SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NJL·September 14, 2022

    NBCA LIQUID EMBOLIC SYSTEM 2

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code KGG·October 4, 2016

    AGILITY HYDROPHILIC STEERABLE GUIDEWIRES

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code DQX·August 8, 2016

    UNKNOWN PEEK INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·October 20, 2022

    UNKNOWN PEEK INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·October 17, 2022

    UNKNOWN PEEK INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·October 17, 2022

    UNKNOWN MANUAL INSTR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code NBH·October 17, 2022

    CRYSTAL AIRWAY MASK

    FDA Adverse Event
    Malfunction ·KOO MEDICAL EQUIPMENT (SHANGHAI) CO. LTD·Product code CAE·February 20, 2015

    TRUFIT CB PLUG

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW MANSFIELD MANUFACTURING SITE·Product code MQV·July 2, 2012

    UNK HIP FEMORAL STEM CORAIL

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LZO·June 5, 2024

    UNK HIP ACETABULAR LINER CERAMIC

    FDA Adverse Event
    Death ·DEPUY ORTHOPAEDICS INC US·Product code LPH·June 5, 2024