BEUDAMED
    12 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 ×

    AMSCO SURGICAL TABLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293326·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049538·K-Wires, Single diamond threaded, .062-inch (1....

    INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EsophyX2 HD Device with SerosaFuse Fasteners and Accessories, EsophyX Z Device with SerosaFuse Fasteners and Accessories

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQC·August 5, 2015

    3.7MM TI CERVICAL SPINE SCREW SLF-DRLG/VARIABLE ANGLE 14MM

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code OVE·February 21, 2013

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 31, 2014

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·September 30, 2023

    ESOPHYX Z

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017

    PALL ULTIPOR 25 BREATHING SYSTEM FILTER

    FDA Adverse Event
    Injury ·PALL NEWQUAY·Product code CAH·July 13, 2018

    PALL ULTIPOR 100 BREATHING SYSTEM FILTER

    FDA Adverse Event
    Injury ·PALL NEWQUAY·Product code CAH·April 18, 2017