BEUDAMED
    1,041 results · 20ms · 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.

    C. DIFFICILE TOX A/B II

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489004042·PowerChem Neoprene Exam Gloves, Large

    TK® Ti-KNOT®

    FDA UDI
    LSI Solutions, Inc.·00850200006094·TK® Ti-KNOT® DEVICE

    Biongraft

    Device
    EU MDD · Eu Md Class 3 ·Bonegraft Biomaterials Co.·On the market·32 countries

    IRVINE BIOMEDICAL. INC.

    FDA registration
    IRVINE BIOMEDICAL. INC.·9 products·🇺🇸 United States

    Mobilio

    FDA UDI
    Ropox A/S·05707581000591·

    MiroDerm Fenestrated Plus

    FDA UDI
    REPRISE BIOMEDICAL, INC.·00857072005217·4 x 4 cm Fenestrated Plus Biologic Wound Matrix

    SUPRASPERM SYSTEM

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

    PC ECG 1200

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    2030404-2011-00274

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, IRVINE·October 12, 2011

    2030404-2018-00067

    FDA Adverse Event
    Injury ·September 18, 2018

    2030404-2010-00083

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, IRVINE·July 29, 2010

    INTRODUCER, ELECTROPHYSIOLOGY

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code DYB·July 25, 2016

    TRANSSEPTAL NEEDLE, BRK SERIES, ADULT 18 GA, 98CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DRC·July 19, 2011

    SWARTZ¿ BRAIDED TRANSSEPTAL GUIDING INTRODUCER, SL1¿, 63 CM LENGTH, 8.5F

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL (AFD-PLYMOUTH)·Product code DYB·July 25, 2016

    AGILIS NXT, 8.5F, STEERABLE INTRODUCER, MED CURL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (AF-IRVINE)·Product code DYB·December 20, 2013

    AGILIS? NXT STEERABLE INTRODUCER DUAL-REACH? 71 CM SHEATH, MEDIUM CURL, 8.5 F

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DYB·October 23, 2014

    BRK? TRANSSEPTAL NEEDLE, 98 CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DRC·October 23, 2014

    FLEXABILITY¿ ABLATION CATHETER, SENSOR ENABLED¿

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code OAD·September 20, 2019

    ADVISOR¿ HD GRID MAPPING CATHETER, SENSOR ENABLED¿

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code DRF·September 20, 2019