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

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    Filters Regulation: Us FDA ×

    BowTie™ SI Joint Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Unity ASC - Distal Resection Guide

    FDA UDI
    ENZTEC LIMITED·09421028113021·A reusable surgical instrument intended to be u...

    RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR

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

    MyndMove 2.0

    FDA 510(k)
    FDA Class 2 ·Neurology

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·June 14, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 22, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·January 10, 2025

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·November 4, 2008

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 2, 2011

    LUMAX 540 VR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·July 17, 2013