BEUDAMED
    15 results · 25ms · Sources: EU EUDAMED, US FDA

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    PACIFIC SURGICAL PATTIES

    FDA 510(k)
    FDA Class 2 ·Neurology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993019·anteriors; shade A1; mould UCL

    Bipolar forceps

    FDA UDI
    SOPRO-COMEG GmbH·04059082014715·

    DANNIK Disposable Monopolar Laparoscopic Instrument

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

    ENAMELITE ACRYSEAL SPRAY SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024162112·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024162105·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024162129·

    TT BASIC HVLP TRACHEOSTOMY TUBE 7.8 MM

    FDA Adverse Event
    Malfunction ·UNOMEDICAL SDN BHD·Product code JOH·March 1, 2013

    ITRAK 3000

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·February 8, 2011

    PROTECTA XT CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 5, 2015

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 9, 2015

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 30, 2018

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026