BEUDAMED
    31 results · 21ms · Sources: EU EUDAMED, US FDA

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    HELENA RISTOCETIN

    FDA 510(k)
    FDA Class 2 ·Hematology

    MGB Alert Internal Control Set IC2-C-480 rxn

    FDA UDI
    Elitechgroup Mdx LLC·03661540951626·The MGB Alert Internal Control Set IC2-C consis...

    Elite Orthopaedics

    FDA UDI
    Elite Orthopaedics, Inc.·00816591013387·Post Op Telescoping Knee Brace

    0800,APS1,08,N,VL,LT,RDL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828153065·0800,APS1,08,N,VL,LT,RDL

    MGB Alert Internal Control Set IC2-C -480 rxn QTY-100

    FDA UDI
    ELITECH GROUP INC.·03661540952302·The MGB Alert Internal Control Set IC2-C consis...

    MGB Alert Internal Control Set IC2-C -480 rxn QTY-25

    FDA UDI
    ELITECH GROUP INC.·03661540952296·The MGB Alert Internal Control Set IC2-C consis...

    ACUMED

    FDA UDI
    Acumed LLC·10806378042140·LE Screw Caddy Cover

    RESPONSE 2000 CEMENTED HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MAPERSOL

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

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·November 3, 2011

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 15, 2012

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 6, 2012

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 28, 2013

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 24, 2013

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·September 20, 2012

    BIODESIGN 4-LAYER TISSUE GRAFT

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code PAG·April 3, 2014

    TRANSITION 2 LEVEL IMPLANT, LORDOSED, 28MM

    FDA Adverse Event
    Injury ·GLOBUS MEDICAL, INC.·Product code NQP·October 16, 2012

    CRE PULMONARY BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KTI·August 16, 2010

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 12, 2014

    Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.

    FDA Recall
    Terminated ·Andover Healthcare Inc.·Product code FQM·June 19, 2019