BEUDAMED
    45 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.

    HIGHLY CROSS-LINKED VITAMIN E UHMWPE TIBIAL INSERTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814268·GENUMEDI PT SILVER R III

    FlexStep

    FDA UDI
    Liftup A/S·05714420032231·FlexStep V2, 900, 3+1 step, outdoor

    HOWARD BONE RASPATORY

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896052321·HOWARD BONE RASPATORY DOUBLE ENDED SINGLE-SIDED...

    Zavation

    FDA UDI
    Zavation LLC·00197157007577·Recessed ALIF Screw Inserter - Free Hand, 23mm

    ENZA-A

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030EZA1032230·Anchor Deployment Ram, Bar Inserter

    Enza-O

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030EZO1032230·Anchor Deployment Ram

    GEON DIGITAL CLINICAL THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PATIENT VENTILATION OXYGEN CONCENTRATING SYSTEM (PVOCS)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM HEPARIN

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·April 27, 2018

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·October 24, 2015

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 3, 2022

    MONARCH III IOL DELIVERY SYSTEM, CARTRIDGE D

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD. - HUNTINGTON·Product code MSS·December 31, 2017

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·July 13, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2016

    VA LOCKSCR Ø2.4 SELF-TAP L12 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 18, 2013

    WALLFLEX? COLONIC

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code MQR·May 9, 2013

    IV ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC·Product code FPA·May 28, 2008

    CARPENTIER-EDWARDS PERIMOUNT AORTIC PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 25, 2011

    VA LOCKSCR Ø2.7 HEAD 2.4 SELF-TAP L14 TA

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·April 27, 2022