BEUDAMED
    57 results · 31ms · 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.

    KARL STORZ Endoscopic Accessories for Urology

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

    Darby Dental Supply, LLC

    FDA UDI
    DARBY DENTAL SUPPLY, LLC·00889813054567·ALGINATE SUBSTITUTE 380ML RS

    Tubing, Smooth Interior, Hytrel, IMC, 22MM-14"

    FDA UDI
    A-M SYSTEMS, LLC·00817081024821·Tubing, Smooth Interior, Hytrel, IMC, 22MM-14"

    Q-FIX

    FDA UDI
    Smith & Nephew, Inc.·00885556724644·2.8MM Q-FIX ALL SUTURE ANCHOR

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702372250·E3/AG/PL-SL-OT-E/NOP5-T-OH/GRE

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2528000010·Dual Headbody, Modular, Polyaxial

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2528000020·Dual Headbody, Modular, Plolyaxial , Reduction

    NIM® 2.0 MAINFRAME

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code IKN·May 16, 2016

    PROVISIONAL INLAY/ONLAY KIT

    FDA 510(k)
    FDA Class 2 ·Dental

    illumigene Mycoplasma DNA Amplification Assay

    FDA 510(k)
    FDA Class 2 ·Microbiology

    INTERFACE 8252800 RESPONSE 2.0 INCREMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code IKN·August 6, 2013

    MAINFRAME 8253001IP RESPONSE 2.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·April 2, 2013

    MAINFRAME 8252001IP RESPONSE 2.0 W/INCRE

    FDA Adverse Event
    Malfunction ·XOMED MFG JACKSONVILLE·Product code ETN·January 4, 2013

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAM·December 4, 2008

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·September 19, 2011

    OPEN SPINE CLAMP, TITANIUM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·July 29, 2013

    INTERFACE 8252800 RESPONSE 2.0 INCREMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·October 16, 2012

    INTERFACE 8252800 RESPONSE 2.0 INCREMENT

    FDA Adverse Event
    Malfunction ·XOMED MFG JACKSONVILLE·Product code ETN·April 11, 2012

    INTERFACE 8252800 RESPONSE 2.0 INCREMENT

    FDA Adverse Event
    Malfunction ·XOMED MFG JACKSONVILLE·Product code ETN·February 27, 2012

    INTERFACE 8252800 RESPONSE 2.0 INCREMENT

    FDA Adverse Event
    Malfunction ·XOMED MFG JACKSONVILLE·Product code ETN·March 27, 2012