BEUDAMED
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    HaWe Industries

    Manufacturer
    🇵🇰 Pakistan

    Haw Par Healthcare Limited

    Manufacturer
    🇸🇬 Singapore·1 Basic UDI-DI·3 Devices·1 Importer

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749023824·CERAMO SCHICK cerebral suction tube,45° angl. u...

    TISSUE PATCHES - OTHER

    Device
    EU MDR · Eu Md Class 1 ·Haw Par Healthcare Limited·On the market·4 countries

    TISSUE PATCHES - OTHER

    Device
    EU MDR · Eu Md Class 1 ·Haw Par Healthcare Limited·On the market·4 countries

    TISSUE PATCHES - OTHER

    Device
    EU MDR · Eu Md Class 1 ·Haw Par Healthcare Limited·On the market·4 countries

    HAW

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC (LITTLETON)·Product code OWB·October 3, 2018

    OPTIVIEW SMALL KIT

    FDA Adverse Event
    Injury ·KERR HAWE SA·Product code EIG·December 16, 2016

    HAWE BRISTLE BRUSHES NYLON

    FDA Adverse Event
    Injury ·KERR HAWE SA·Product code EHL·October 25, 2016

    OPTIVIEW SMALL KIT

    FDA Adverse Event
    Injury ·KERR HAWE SA·Product code EIG·December 16, 2016

    OPITVIEW SMALL KIT

    FDA Adverse Event
    Injury ·KERR HAWE SA·Product code EIG·February 9, 2021

    OPITVIEW SMALL KIT

    FDA Adverse Event
    Injury ·KERR HAWE SA·Product code EIG·February 8, 2021

    OPTIVIEW SMALL KIT

    FDA Adverse Event
    Injury ·KERR HAWE SA·Product code EIG·February 8, 2021

    OPTIVIEW

    FDA Adverse Event
    Injury ·KERR HAWE S.A·Product code EIG·October 18, 2019

    OPTIVIEW

    FDA Adverse Event
    Injury ·KERR HAWE S.A·Product code EIG·October 18, 2019

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·November 10, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·April 11, 2018

    NEXGEN COMPLETE KNEE SOLUTION MIS TOTAL KNEE PROCEDURE TIBIAL BROACH IMPACTOR

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HWA·January 9, 2009