BEUDAMED
    43 results · 24ms · Sources: EU EUDAMED, US FDA

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    Invictus™ OsseoScrew® System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113332·PHACO KNIFE 3.0MM ANGLED (BX/5)

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113349·PHACO KNIFE 3.2MM ANGLED (BX/5)

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113325·PHACO KNIFE 2.8MM ANGLED (BX/5)

    CLEARVISION DR 7000F

    FDA 510(k)
    FDA Class 2 ·Radiology

    NOVUS SPECTRA

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

    BLOOD PUMP PU VALVES 15 ML, IN/OUT Ø9 MM

    FDA Adverse Event
    Injury ·BERLIN HEART GMBH·Product code DSQ·June 21, 2023

    BLOOD PUMP PU VALVES 15 ML, IN/OUT Ø9 MM

    FDA Adverse Event
    Injury ·BERLIN HEART GMBH·Product code DSQ·June 21, 2023

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020

    AMPLATZER AMULET

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NGV·October 26, 2023

    AMPLATZER AMULET

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NGV·October 26, 2023

    BREAST IMPLANTS

    FDA Adverse Event
    Injury ·UNK·Product code FWM·October 16, 2008

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·August 8, 2011

    GYNECARE TVT SYSTEM

    FDA Adverse Event
    Injury ·JOHNSON AND JOHNSON - ETHICON·Product code OTN·June 27, 2013

    TRUE METRIX

    FDA Adverse Event
    Injury ·TRIVIDIA HEALTH INC·Product code NBW·October 18, 2023

    FLEXCATH ADVANCE STEERABLE SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·July 3, 2024

    ACHIEVE ADVANCE MAPPING CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DRF·July 3, 2024

    PERCLOSE PROGLIDE¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·May 12, 2026

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·April 8, 2021

    CD HORIZON SOLERA VOYAGER SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·May 27, 2024