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

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    MONICA AN24

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    EVOTECH™

    FDA UDI
    ADVANCED STERILIZATION PRODUCTS SERVICES INC.·10705037000302·Channel Connector Tube, Brown

    Preci-Vertix

    FDA UDI
    Preat Corporation·00842092155585·Preci-Vertix Kit. Kit contains:. 6 Hader Yellow...

    eTRAX™ Needle System Starter Kit

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436103428·Reusable non-sterile needle sensor with sterile...

    L1

    FDA UDI
    KLS-Martin L.P.·00888118142078·BASE, UNIVERSAL, SCREW LEVEL

    FUTURA TOPCAP NON GAMMA-2

    FDA 510(k)
    FDA Class 2 ·Dental

    STEATHSTATION TREATMENT GUIDANCE PLATFORM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Simpact Tri-Fin

    FDA UDI
    Life Spine, Inc.·00190837063337·Anterior Curette #1 Ang 9" Handle

    Widex

    FDA UDI
    Widex A/S·05706069722185·Widex D-PA BTE (Warm beige S-110 ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069721805·Widex D-FS BTE (Warm beige S-110 ) Telecoil, RC...

    Widex

    FDA UDI
    Widex A/S·05706069720716·Widex UNIQUE U-PA BTE (Warm beige S-110 ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069720990·Widex BEYOND B-F2 (Warm beige S-110 ) Telecoil,...

    Widex

    FDA UDI
    Widex A/S·05706069720082·Widex D-9 BTE (Warm beige S-110 ) Telecoil, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069721485·Widex UNIQUE U-FS BTE (Warm beige S-110 ) Telec...

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·June 12, 2025

    REMOVABLE EXTENSION ARM-FLEX 30MM FOR CMF DISTRACTOR

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MQN·May 9, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011

    SHILEY LOW PRESSURE CUFFED

    FDA Adverse Event
    Injury ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code BTO·August 6, 2008

    UNKNOWN CHLORAPREP

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXG·September 21, 2021

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 6, 2019