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

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    Spinal Elements Ti-Bond coated devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780362661·Integra® Miltex® McPherson Needle Holder, With ...

    mambo™ modular cervical plate system

    FDA UDI
    Ulrich GmbH & Co. KG·04052536008063·mambo plate XS violet, 6-hole, length 37 mm

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    AVEA VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACL TIGHTROPE DOUBLE BUNDLE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HT70 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS·Product code CBK·June 14, 2013

    HEARTSTART MRX EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·August 4, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 28, 2011

    VIASYS

    FDA Adverse Event
    Other ·CAREFUSION 207, INC·Product code CBK·October 27, 2009

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    PENUMA IMPLANT

    FDA Adverse Event
    Injury ·INTERNATIONAL MEDICAL DEVICES, INC.·Product code MIB·October 7, 2019

    MUST MINI OC PRE-BENT TRANSITION ROD 75° Ø3.5/4X 200MM (STE)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKG·April 25, 2024