BEUDAMED
    35 results · 24ms · 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 ×

    WEBSTER DUO-DECAPOLAR CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964073014·Endo Carry-On Procedure Kit

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00850038691011·

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365106255·

    TITAN POROCOAT HIP PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO MEDRAD SPECTRIS MR INJECTOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TSRH SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code KWP·May 19, 1999

    SUMMIT POR TAPER SZ6 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·June 21, 2018

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 6, 2013

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 19, 2014

    CONSTELLATION

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 18, 2011

    SUMMIT POR TAPER SZ4 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·June 20, 2018

    SUMMIT POR TAPER SZ6 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDIC INC, 1818910·Product code LPH·June 1, 2018

    SUMMIT POR TAPER SZ4 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 28, 2018

    LGC TIBIAL FIT TRAY CEM SZ 3.5F / 3.5T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 6, 2025

    SUMMIT POR TAPER SZ7 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 18, 2019

    SUMMIT POR TAPER SZ4 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. - 8010379·Product code LPH·July 1, 2015

    LOGIC FEMORAL PS CEM RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 4, 2024

    OPTETRAK HI-FLEX TIBIAL INSERT SZ 4 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 25, 2022

    PINN CAN BONE SCREW 6.5MMX15MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018