BEUDAMED
    22 results · 34ms · Sources: EU EUDAMED, US FDA

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    PASSPORT 2 WITH VIEW 12 ECG ANALYSIS MODULE MODEL # 0998-00-0170-XXXX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074027364·BONE SCREW 7020550 ILIAC 5.5X50 SS

    Channels

    FDA UDI
    HENRY SCHEIN, INC.·10304040160746·Channels Flex 25mm 20.04

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717107177·Gutta Percha Points, Taper .04, Size #45, 60pcs...

    KARL STORZ ENDOSCOPY-AMERICA, INC.

    FDA registration
    KARL STORZ ENDOSCOPY-AMERICA, INC.·207 products·🇺🇸 United States

    3M™ Unitek™ Uni-Twin™

    FDA UDI
    3M UNITEK CORPORATION·00652221016478·Mini Uni-Twin(TM) Bracket LR3 -7T/6A .022 5/Pk

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code EZO·July 7, 2011

    RDH BANDAGE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OTW MEGALINK SDS BILIARY STENT SYSTEM

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

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·March 16, 2021

    CUTTING LOOP, BIPOLAR, 26 FR.

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code HIN·August 11, 2025

    CUTTING LOOP, BIPOLAR, 26 FR.

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code HIN·August 11, 2025

    TWO-PEDAL FOOTSWITCH HF GENERATORS

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code GEI·April 21, 2025

    BIPOLAR HIGH FREQUENCY CORD, 400 CM

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code GEI·November 26, 2025

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code FPK·March 5, 2007

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·March 26, 2013

    OXIMAX N-595 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code DQA·February 10, 2011

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·March 28, 2008

    CLAMPING JAW, SMALL

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code OCV·May 16, 2023

    BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·April 21, 2021