BEUDAMED
    22 results · 23ms · 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 ×

    OSTEONICS 7000 SERIES TOTAL KNEE TIBIAL COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756389624·BREAST PACK

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112359·SURG-I-BAND PURPLE GLOW

    NA

    FDA UDI
    STERILMED, INC.·10888551007542·SAW BLADE SAGITTAL K9 K2000 SERIES

    GSO ACP1 ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMS SLING FIXATION SYSTEM

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

    S3 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR)·Product code DTQ·April 23, 2010

    3 TO 1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 14, 2011

    S3 ROLLER PUMP MODULE AND CONSOLE

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR·Product code DTQ·March 24, 2010

    3-TO-1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHMAND·Product code DTQ·December 14, 2011

    STOCKERT S3 CONSOLE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·October 6, 2011

    STOCKERT S3 CONSOLE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·October 6, 2011

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·November 23, 2010

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·January 11, 2013

    FORTIFY ASSURA VR, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 2, 2014

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·HEART VALVES SANTA ANA·Product code DYE·December 6, 2021

    SENSOR, LOW LEVEL II

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 16, 2010

    S3 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR)·Product code DTQ·April 23, 2010

    S3 ROLLER PUMP

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 22, 2010

    S3 ROLLER PUMP

    FDA Adverse Event
    SORIN GROUP DEUTSCHLAND·Product code DWB·October 12, 2016