BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MONDEAL

    FDA UDI
    MONDEAL Medical Systems GmbH·04050435060939·MCD Screw 2.0 x 16 mm M1 non lo...

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113393·PS Insert, Size 6 x 16mm

    BAYER RAPIDPOINT 405 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    SPACELABS HEALTHCARE QUBE COMPACT MONITOR (91390

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COBAS 8000 E602 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 20, 2014

    ADVIA CENTAUR CP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·November 6, 2012

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code FZP·September 13, 2007

    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

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015