BEUDAMED
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    UbiqVue™ 2A Multi-parameter System (UX2550)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MITEK

    FDA UDI
    Medos International Sàrl·10886705029150·HD EP Arthroscope/Sinuscope compatible with Mit...

    Symmetry Charnley

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482061190·Symmetry® Blade; Charnley Retractor; Rounded; 2...

    n/a

    FDA UDI
    Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM59002421060181·Rotary instrument for ENT surgery

    Ophthalmic Scissors

    FDA UDI
    KATENA PRODUCTS, INC.·00841668105191·HOLLAND DALK SICISSORS RIGHT

    SKYHAWK

    FDA UDI
    Orthofix US LLC·18257200087679·SKYHAWK PLATE IMPLANTS, SIZE 18

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197307154·Citelli-Beyer Bone Punch 3 4/3"...

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517074109·

    Hill-Rom Heart and Respiration Rate Monitoring System: Single Sensor, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Packs, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Activation

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACUTE PORTABLE EXCHANGE DEIONIZATION (PEDI) SYSTEM, CENTRAL PEDI SYSTEM, BACK-UP PEDI SYSTEM

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

    ASKU

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·April 24, 2018

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

    CAPD SOLUTION TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

    SMITHS MEDICAL PORTEX® ENDOTRACHEAL TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code CBI·April 18, 2019

    SMITHS MEDICAL PORTEX® ENDOTRACHEAL TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code CBI·April 18, 2019

    SABRATEK

    FDA Adverse Event
    Injury ·SABRATEK CORP.·Product code FPA·May 14, 1998

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·October 23, 2018

    CONSERVE(R) PLUS CUP

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code KWA·October 23, 2018

    NUCLEUS FREEDOM IMPLANT WITH STRAIGHT ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LIMITED·Product code MCM·December 23, 2018