BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    Triton

    FDA 510(k)
    FDA Unclassified ·Unknown

    NA

    FDA UDI
    Synthes GmbH·10886982151513·2.4MM CANNULATED SCREW LONG THREAD 13MM

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF2118130·2.4mm Cannulated Screw, Long Thread, 13mm

    Diamond Orthopedic, LLC

    FDA UDI
    DIAMOND ORTHOPEDIC, LLC·B551DMD2118130·2.4mm, Cannulated Screw, Long Thd., 13mm

    Medical Surgical Mask

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

    AMEDITECH IMMUTEST DRUG SCREEN THC

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ALARIS® PUMP MODULE

    FDA Adverse Event
    Injury ·CAREFUSION·Product code FRN·December 21, 2016

    HEMODIALYSIS KIT: 2-L 15 FR X 28 CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code MSD·July 20, 2011

    INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 29, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 8, 2013

    Model Number L211 PROPONENT DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025

    PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL MRI (Model Number L211), EL (Model Number L221), and EL MRI (Model Number L231).

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·January 22, 2025