BEUDAMED
    70 results · 23ms · 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.
    Filters Regulation: Us FDA ×

    Teleport Microcatheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517576026·CoRoent Ant TLIF Ti, 8x12x36mm 0°

    Ophthalmic Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100981·DESMARRES LID RETRACTOR #3

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916148645·ZEUS®-L 60 x 23 x 18mm 28 Degree

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916120702·ZEUS®-L 60 x 23 x 18mm 14 Degree

    ICESENCE 3

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

    QUADROX-I MICROPORPOROUS MEMBRANE OXGENATOR SERIES AND QUDROX-ID DIFFUSION MEMBRANE OXYGENATORS SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BE-PLS 2050

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 26, 2014

    BE-PLS 2050 PERMENANT LIFE SUPPORT

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KFM·March 6, 2014

    BE-PLS 2050 PERMENANT LIFE SUPPORT

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 27, 2014

    HLS SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·August 18, 2025

    TUBING SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·April 28, 2025

    TUBING SET

    FDA Adverse Event
    Death ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·April 28, 2025

    TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·January 20, 2026

    TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·January 20, 2026

    EXCEL 36KHZ STRAIGHT HANDPIECE

    FDA Adverse Event
    Malfunction ·INTEGRA, ANDOVER·Product code LFL·July 11, 2011

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 10, 2013

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·August 8, 2014

    BE-PLS 2050 PERMANENT LIFE SUPPORT

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 20, 2014

    BE-PLS 2050 PERMENANT LIFE SUPPORT

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 28, 2014