BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Cardioblate CryoFlex Surgical Ablation System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POWER-FREE NITRILE PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SFI-BAR

    FDA 510(k)
    FDA Class 2 ·Dental

    ATHLETE I/A TIP 45 DEGREE TYPE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQC·June 26, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·July 27, 2011

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS CORP.·Product code LFR·September 26, 2008

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·December 14, 2023

    BIO-COMP SWIVELOCK C, CLD 5.5X19.1MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MAI·April 22, 2020

    BD MICROTAINER® TUBES WITH K2E (K2EDTA)

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·July 9, 2019

    BD MICROTAINER® TUBES WITH K2E (K2EDTA)

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·July 10, 2019

    BD MICROTAINER® TUBES WITH K2E (K2EDTA)

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·July 11, 2019