BEUDAMED
    31 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 Regulation: Us FDA ×

    VISION R/F TILTING TABLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    CUSTOM PROCEDURE KIT

    FDA UDI
    MEDIVATORS INC.·40677964004344·CUSTOM PROCEDURE KIT

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317302120·

    TruFlex™

    FDA UDI
    Ortho Organizers, Inc.·00190707125608·TRUFLEX NiTi RCS Type 5 Lower 020 (10pk)

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730013798·NiTi RCS Type 5 Lower 020 10 archwires per pack

    Sonoclot® gbACT+ Kit

    FDA UDI
    SIENCO, INC.·B55880004121·The gbACT+ Kit is an in vitro diagnostic reagen...

    CURE 2.0 ACP

    FDA UDI
    SpineArt SA·07640332475478·DOUBLE BARREL DRILL GUIDE 2 - FIXED

    CURE 2.0™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B1671000412000·

    Attacha Vac

    FDA UDI
    I.C. MEDICAL, INC.·00817688021216·

    IMMULITE PHENOBARBITAL, MODELS LKPB1, LKPB5

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ACUCAM CONCEPT IV, MODELS A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401

    FDA 510(k)
    FDA Class 1 ·Dental

    CODEMASTER

    FDA Adverse Event
    Malfunction ·AGILENT TECHNOLOGIES/CARDIAC PRODUCTS DIV·Product code LDD·October 23, 2000

    WALLACH ULTRA FREEZE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·September 6, 2022

    TRILOGY BONE SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER, TURPEAUX INDUSTRIAL PARK·Product code LPH·February 16, 2016

    ADVIA CENTAUR XP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JJE·March 12, 2013

    ENCORE BALLOON CATHETER INFLATION DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code MAV·February 24, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·February 20, 2008

    EVIS EXERA GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDS·September 23, 2024

    EVOLUTION ELECTRONIC CONCERVER

    FDA Adverse Event
    Injury ·INOVO. INC·Product code NFB·May 31, 2017

    BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView SPECT is a gamma camera designed for single or dual detector nuclear imaging accommodating a broad range of emission computed tomography Emission Computed Tomography (ECT) studies.

    FDA Enforcement
    Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·June 12, 2013