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

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    Filters Regulation: Us FDA ×

    Zimmer Biomet Ceramic Heads (22.2mm diameter)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Darby Dental Supply, LLC

    FDA UDI
    DARBY DENTAL SUPPLY, LLC·00889813034804·K-Type Files 25MM #40

    devemed

    FDA UDI
    devemed GmbH·04061644033942·Bone Spreader | 3.4 - 4.0 mm straight, graduate...

    NA

    FDA UDI
    aap Implantate AG·04042409445286·Cannulated Headless Bone Screw 2.5, L 34, TL 8 ...

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 20, 2026

    Lever Action Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Atrax Anterior Cervical Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 1, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FOZ·April 6, 2026

    HEARTSTREAM XLT

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 25, 2008

    COATED VICRYL

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAM·September 7, 2011

    CONSERVE(R) PLUS SPIKED CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·July 29, 2013