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

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    Varian High Energy Linear Accelerator, UNIQUE, Varian Multileaf Collimator

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517576002·CoRoent Ant TLIF Ti, 8x11x40mm 4°

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780361756·Integra® Miltex® Iris Scissors 4-1/8", Straight...

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515025707·Brunner Ret, 120 x 25mm, 10 3/4", (27.5cm) Blad...

    Origin Coxa Vara Hip Stem

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215013196·

    Origin Hip Stem, Coxa Vara

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215051884·

    Paxeon Origin Coxa Vara Hip Stem

    FDA UDI
    PAXEON RECONSTRUCTION LLC·08177570200573·Origin Stem, Coxa Vara Size 14

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161111814040·Coxa Vara Collared Stem, Size 14

    SPINAL INTEGRATION SPINAL-EZE INTRAOPERATIVE EPIDURAL CATHETER KIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HUIBAO BODY FAT SCALE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STRATUS Stem

    FDA UDI
    AMPLITUDE SAS·03701089521475·

    ARTIS ZEE III CEILING

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·May 17, 2024

    ARTIS ZEE III CEILING

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·December 3, 2024

    ARTIS Q ZEEGO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·September 29, 2025

    ARTIS ZEE III CEILING

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·April 29, 2026

    ARTIS ZEE III CEILING

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·April 1, 2026

    ARTIS ZEEGO III (CHINA)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·December 26, 2023

    LOFRIC NELATON CH10

    FDA Adverse Event
    Injury ·WELLSPECT HEALTHCARE·Product code KOD·June 14, 2013

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·July 21, 2011

    PKG STRL VALV PUD, 12MM, L.P.

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES, PR·Product code JXG·September 24, 2008