BEUDAMED
    29 results · 20ms · Sources: EU EUDAMED, US FDA

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    BREAST IMMOBILIZATION DEVICE MR-BY 160

    FDA 510(k)
    FDA Class 2 ·Radiology

    DP97

    FDA UDI
    Denplus Inc·D8451001303·DP97, RPI, 11.3 kg

    PERMITE

    FDA UDI
    SDI LIMITED·09336472000288·PERMITE 1SP REG 50

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001303·artVeneer life upper anteriors, BS, C1

    PERMITE

    FDA UDI
    SDI LIMITED·DO3640013032·

    Health-Tec/DHP Hand Instruments

    FDA UDI
    Dental Health Products Inc·D77370013030·Health-Tec/DHP Explorer DE 5

    Scanlan® TIP-GUARD™ instrument protectors - Tinted

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159002027·Scanlan® TIP-GUARD™ instrument protectors - Ori...

    Threshold V2 Pedicular Fixation System

    FDA UDI
    SPINEOLOGY INC.·M7401001303·Rod Pusher

    BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 32 SIZE S

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 30, 2020

    HEALTHCARE SERVICE AND SUPPLY ALP ALTERNATING LEG PRESSURE PUMP AND GARMENTS FOR THE LIMB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Z-NET

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    MPACT ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·March 10, 2026

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    WAVEWRITER ALPHA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 6, 2024

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    ENDO STITCH POLYSORB 0 48 VIO DLU SU

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SUR·Product code KOG·March 6, 2013