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

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    TRYPTIK2C-plate Anterior Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704284980·CALIPER CASTROVIEJO 40 MILLIMETER GRADUATED 6.5"

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704921086·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100288·SAUER PREMATURE INFANT SPECULUM 2MM

    Trulink

    FDA UDI
    STATCORP MEDICAL·10841522130540·BP CUFF,SL,SOFT,1T,SMALL ADULT PLS,23-28,HP,5/BG

    ATMOS E 201 THORAX AND ATMOS S 201 THORAX

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDRAD 1.5T PELVIC IMAGING SYSTEM INTERFACE DEVICE

    FDA 510(k)
    FDA Class 2 ·Radiology

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., HU·Product code KWP·October 17, 2025

    CD HORIZON BALLAST SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·December 9, 2019

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 8, 2014

    VITATRON DA+ T-SERIES DR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code DXY·June 8, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·July 7, 2011

    CHROMID STREPTO B AGAR

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code PQZ·November 1, 2017

    CHROMID STREPTO B AGAR

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code PQZ·November 1, 2017

    COR/TRI ANT STEM INSERT SHAFT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWR·March 10, 2026

    DEPUY PINNACLE ACETABULAR CUP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code ---·December 10, 2019

    ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023