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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    CORTEK CYSTOSCOPE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ODYSSEY®

    FDA UDI
    Microport Orthopedics Inc.·M684K00012971·

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741028854·Catheter Placement Kit

    GC Fuji II LC®

    FDA UDI
    Gc America Inc.·14548161282376·GC Fuji II LC® A3, 15 g powder btl

    GC Fuji II LC®

    FDA UDI
    Gc America Inc.·D0470001971·GC Fuji II LC® A3, 15 g powder btl

    intellijoint HIP®

    FDA UDI
    Intellijoint Surgical Inc·00628184001974·Probe, G2

    AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE

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

    GSI 2000 MIDDLE EAR ANALYZER

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    RADOVAN TISSUE EXPANDER, 700 CC

    FDA Adverse Event
    MENTOR CORP.·Product code LCJ·December 21, 1993

    VOGUE NATURAL Y LOW PROFILE SILASTIC, SIZE 10, SIZE 8

    FDA Adverse Event
    MEDICAL ENGINEERING CORP.·Product code FTR·December 21, 1993

    VERCISE GENUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·August 30, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·July 5, 2023

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·February 25, 2025

    EMAX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBE·February 14, 2013

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·February 3, 2011

    DURDURT TS TIB INSMED 13MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code HSH·February 19, 2008

    ACCESS® 2 IMMUNOASSAY SYSTEM, REFURBISHED

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JJE·January 30, 2012

    ACCESS® 2 IMMUNOASSAY SYSTEM, REFURBISHED

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JJE·January 30, 2012

    ACCESS® 2 IMMUNOASSAY SYSTEM, REFURBISHED

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JJE·January 30, 2012

    ACCESS® 2 IMMUNOASSAY SYSTEM, REFURBISHED

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JJE·January 30, 2012