BEUDAMED
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    SERIM DISINTEK GTA 2.1%, MODEL: 5164

    FDA 510(k)
    FDA Class 2 ·General Hospital

    258336

    FDA Adverse Event
    Malfunction ·December 22, 1999

    ETHICON

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY·Product code KOG·January 9, 2004

    Serim® DISINTEK™ GTA 1.5% Test Strips

    FDA UDI
    SERIM RESEARCH CORPORATION·M1745136A1·Serim DISINTEK GTA 1.5% Test Strips are used to...

    SERIM D-CIDE GTA 1.5% TEST STRIP, MODEL PART NUMBER 5171

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GTA INFRARED HEATING PAD

    FDA Adverse Event
    Injury ·UNKNOWN·Product code IRT·March 6, 2019

    4 WHEELED SCOOTER

    FDA Adverse Event
    Injury ·Product code INI·August 14, 2014

    ETS LINEAR CUTTER STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 21, 2014

    GTA 75 RELOADABLE LINEAR CUTTER WITH SAFETY LOCK-OUT

    FDA Adverse Event
    Malfunction ·ETHICON·Product code GCJ·September 18, 2015

    EVIS EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·September 21, 2023

    JOEY 1000ML PUMP SET

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code LZH·December 19, 2016

    GORE DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code FTL·August 29, 2019

    PRESIDIO 18 - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code HCG·September 4, 2015

    DRILL BIT WIRE-PASS M DIAMETER 1.5MM X 7.0MM

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code ERL·November 20, 2020

    POWERPICC CATHETER W/ SHERLOCK 3CG (TPS) STYLET 4F FULL TRAY

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·June 17, 2024

    EVOLUT FX PLUS VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·November 19, 2024

    CIDEX OPA SOLUTION

    FDA Adverse Event
    Death ·ADVANCED STERILIZATION PRODUCTS·Product code MED·August 26, 2016

    Antisera, All, Serratia Marcesans

    FDA classification
    FDA Class 1 ·Antisera, All, Serratia Marcesans

    INFINITUM ETA LTD.

    FDA registration
    INFINITUM ETA LTD.·4 products·🇮🇱 Israel

    GDA MARKETING LIMITED

    FDA registration
    GDA MARKETING LIMITED·2 products·🇭🇰 Hong Kong