BEUDAMED
    61 results · 82ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    INTROCAN SAFETY®

    FDA Adverse Event
    Injury ·B. BRAUN MELSUNGEN AG·Product code DYB·March 27, 2019

    12X150MM KII SHIELDED BLADED ACCESS SYS THREADED

    FDA Adverse Event
    APPLIED MEDICAL·Product code GCJ·July 8, 2011

    GORE® TAG® CONFORMABLE THORACIC STENT GRAFT WITH ACTIVE CONTROL SYSTEM

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·November 14, 2025

    UNIMAX ENDO POUCH WITH MEMORY WIRE 3X6

    FDA Adverse Event
    Malfunction ·UNIMAX MEDICAL SYSTEMS, INC.·Product code GCJ·November 19, 2019

    FREESTYLE COMFORT

    FDA Adverse Event
    Malfunction ·CAIRE INC.·Product code CAW·September 1, 2022

    HYDROFRAME-18-AV

    FDA Adverse Event
    Injury ·MICROVENTION, INC.·Product code KRD·January 8, 2026

    OPTICAL INTEGRITY GENERAL SHAPED FIBER

    FDA Adverse Event
    OPTICAL INTERGRITY INC.·Product code GEX·March 15, 2012

    MICRUSPHERE XL 8MMX25CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·August 20, 2019

    GORE® EXCLUDER®AAA ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·November 15, 2022

    HYDROMARK BREAST BIOPSY SITE MARKER

    FDA Adverse Event
    Injury ·DEVICOR MEDICAL PRODUCTS, INC.·Product code NEU·August 15, 2019

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·August 2, 2016

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 30, 2018

    LANTIS COMMANDER 10 USER

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code LNX·June 27, 2006

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 7, 2016

    INTROCAN®-W

    FDA Adverse Event
    Injury ·B BRAUN MELSUNGEN AG·Product code FOZ·May 15, 2024

    CUSTOM MADE RELAY PRO THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·December 2, 2024

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK ENDOSCOPY·Product code FGE·September 14, 2018

    ION

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code EOQ·February 15, 2024

    RELAY PRO NBS THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·March 19, 2026

    GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code NIP·January 23, 2025