BEUDAMED
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    RESOUND

    FDA Adverse Event
    Injury ·GN HEARING A/S·Product code OSM·December 6, 2019

    PDS II (POLYDIOXANONE) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GNH·January 28, 2005

    CADD ADMINISTRATION SETS - FLOW STOP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·April 29, 2021

    PERFUSOR SPACE

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·May 4, 2023

    Antigen, Fluorescent Antibody Test, Schistosoma Mansoni

    FDA classification
    FDA Class 1 ·Antigen, Fluorescent Antibody Test, Schistosoma Mansoni

    GNI Co., LTD

    FDA registration
    GNI Co., LTD·21 products·🇰🇷 South Korea

    VITEK® 2 NH ID TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JST·February 10, 2017

    GNS (BAGO) HEALTHCARE COMPANY LIMITED

    FDA registration
    GNS (BAGO) HEALTHCARE COMPANY LIMITED·1 product·🇲🇲 Myanmar

    FRESNEL PRISM AND LENS

    FDA UDI
    Fresnel Prism & Lens Company·00850029104278·TRIAL RING - 2 DIOPTER NO HANDLE

    NA

    FDA UDI
    SOUTHERN IMPLANTS (PTY) LTD·06009544021872·Titanium Abutment, Non-Engaging, for Max9 Ex He...

    ExHex

    FDA UDI
    KEYSTONE DENTAL, INC.·D768TCMAX91NH0·Temp Sleeve

    NA

    FDA UDI
    SOUTHERN IMPLANTS (PTY) LTD·06009544025498·Temporary Peek Abutment, Non-Engaging, for Max9...

    FRESNEL PRISM AND LENS

    FDA UDI
    Fresnel Prism & Lens Company·00850029104285·TRIAL RING - 3 DIOPTER NO HANDLE

    WALTER WISSING & CO. INH. OLAF LAUER

    FDA registration
    WALTER WISSING & CO. INH. OLAF LAUER·2 products·🇩🇪 Germany

    WIDEX HEARING AID #G2H & G2T

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    MODELS G6H, G6T, G1H & G1T

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    GBH-MED

    FDA UDI
    Gvm - US Inc·00850022699115·The mesh ultrasonic nebulizer is a device inten...

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93083908020NH0·Custom 8" Micro Decker/Needle Holder 2mm Str

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93083709011NH0·Bayonet Needleholder

    VITEK® 2 NEISSERIA-HAEMOPHILUS TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code JTO·December 2, 2015