BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    ARROWG +ARD BLUE PLUS ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TIPCONTROL

    FDA UDI
    Richard Wolf GmbH·04055207054178·RF INSTRUMENT BIPO Ø 2.5MM WL 280MM for endosc...

    TIPCONTROL

    FDA Adverse Event
    Injury ·RICHARD WOLF GMBH·Product code GEI·September 8, 2023

    EMDS CREATINE KINASE ITEM NIMBER 65411

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ACCUMAX

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

    7.0MM TI MATRIX POLYAXIAL SCREW 40MM THREAD LENGTH

    FDA Adverse Event
    Malfunction ·SYNTHES (USA) BRANDYWINE·Product code NKB·November 25, 2013

    2.0MM TI CORTEX SCREW COARSE PITCH SELF-TAPPING 6MM

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code JEY·March 7, 2013

    ENRHYTHM MRI

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NVZ·August 8, 2014

    EON MINI IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 6, 2011

    I-STAT ACT KAOLIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code JBP·July 23, 2024