BEUDAMED
    91 results · 28ms · 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 ×

    XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set

    FDA 510(k)
    FDA Class 2 ·Neurology

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180157880·ELMED NATHANSON STYLE LIVER RETRACTORS, 6.5MM D...

    Symmetry Nathanson

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482077757·Retractor, Liver, 6.5 mm Diameter, Large, Natha...

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776208820·Nathanson Liver Retractor Large

    Introcan Safety ® 2

    FDA UDI
    B. BRAUN MEDICAL INC.·04046955745821·INTROCAN SAFETY 2 W PUR 24GX19MM - US

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377021312·Perfect Fit™II R/S Interface Module Cable, Ches...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180160361·Elmed Nathanson Style Liver Retractors 6.5mm Di...

    INFINITY TRIDENT NMT POD

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FDR D-EVO II FLAT PANEL DETECTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962161715·SHORT BLADE, 2 3/8" WIDE, 1 1/4" DEEP

    MINICAP PD TRANSFER SET (EASY-LOCK) WITH TWIST CLAMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 25, 2006

    VITALITY DR

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·August 9, 2006

    AMS SPHINCTER 800 URINARY PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code MIP·March 12, 2013

    SCORPIO-FLEX PS TIBIAL TRIAL

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·December 16, 2010

    CORAIL AMT COLLAR SIZE 11

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code LZO·March 10, 2023

    3.0MM TI-SCREWANCHOR1BLUE SUTU

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·May 4, 2018

    3.0MM TI-SCREWANCHOR1BLUE SUTU

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·March 15, 2018

    ONE TOUCH ULTRA

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code CFR·October 1, 2003

    BENCHMARK XT

    FDA Adverse Event
    Malfunction ·VENTANA MEDICAL SYSTEMS, INC.·Product code KPA·May 28, 2008

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·April 5, 2017