BEUDAMED
    7 results · 22ms · 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 FDA Adverse Event ×

    COMPREHENSIVE REVERSE E1 44-36 STD HMRL BRNG

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PAO·December 11, 2018

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 14, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 17, 2011

    MERIT CUSTOM KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC·Product code DQO·July 24, 2013

    (25-2440) XIVE TG PLUS IMPL D3.8/L8

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLU IH AB)·Product code DZE·February 16, 2021

    BD VACUTAINER® PST¿ GEL AND LITHIUM HEPARINN 83 UNITS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·April 16, 2026

    (25-2440) XIVE TG PLUS IMPL D3.8/L8(IMPLANTS)

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·July 2, 2021