BEUDAMED
    100 results · 36ms · Sources: EU EUDAMED, US FDA

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    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·AL-47 SOFT CONTACT LENS

    Ultraverse® 018

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741156892·Ultraverse® 018 PTA Balloon Dilatation Catheter...

    DRAPE, SURGICAL

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

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AUTIMA(TM) MODEL 2251 & MODEL 2600

    Stimulator, Functional Neuromuscular, Scoliosis

    FDA Pre-Market Approval
    FDA Class 3 ·SCOLITRON(TM) STIMULATOR

    SMALL BATTERY DRIVE

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code HWE·May 20, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 6, 2012

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GFA·August 24, 2010

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AURORA/QUADRA, REFLEX, SIMPLEX,META PACEMAKERS

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AURORA/QUANDRA,REFLEX,SIMPLEX AND META PACEMAKERS

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AUTIMA(TM) MODEL 2251 & MODEL 2600

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AUTIMA(TM) MODEL 2251 & MODEL 2600

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AUTIMA(TM) MODEL 2251 & MODEL 2600

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AUTIMA(TM) MODEL 2251 & MODEL 2600

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AUTIMA(TM) MODEL 2251 & MODEL 2600

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AUTIMA(TM) MODEL 2251 & MODEL 2600

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·REFLEX MODEL 8223E DUAL CHAMBER PULSE GENERATOR

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CETA DDD MODEL 1230 PACER

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·AUTIMA MODEL 2251 GENERATOR & MODEL 2600 PROGRAMME

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·REFLEX MODEL 8223E