BEUDAMED
    45 results · 24ms · Sources: EU EUDAMED, US FDA

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    I-LOGIC INREACH SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814671·GENUMEDI SILVER SIZE IV

    PRINCETON

    FDA UDI
    Princeton Medical Group, Inc.·00810158217546·CLAMP HARKEN ATRAUMA AURICLE ANGLED 9.5"

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434557·Tasso+ convenience kit allows self-collection o...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383556668·Gutta Percha Points is used to root canal filin...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383502740·Gutta Percha Points is used to root canal filin...

    CENTURION 2000 CENTRAL STATION ARRHYTHMIA PATIENT MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OTIS -C PLUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 10, 2020

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 10, 2024

    2.4MM VA LOCKING SCREW STARDRIVE 22MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·June 25, 2013

    VERCISE? CARTESIA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code MHY·October 15, 2025

    VA LOCKSCR Ø2.4 SELF-TAP L18 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HRS·July 15, 2013

    HT70 PLUS VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·May 1, 2013

    PORTEX SPINAL ANESTHESIA TRAYS

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code CAZ·September 12, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·May 20, 2011

    CD HORIZON® FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·September 3, 2024

    CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025

    CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025

    CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·April 2, 2025