BEUDAMED
    10,000 results · 53ms · Sources: EU EUDAMED, US FDA

    EZ Plus Implant System

    FDA registration
    Megagen Implant Co., Ltd.·1 product·🇰🇷 South Korea

    LASER PER FISIOTERAPIA LASERIX PH12

    Device
    EU MDD · Eu Md Class 2b ·GN MED s.r.l.·On the market·1 country

    LASER PER FISIOTERAPIA LASERIX PH3

    Device
    EU MDD · Eu Md Class 2b ·GN MED s.r.l.·On the market·1 country

    LASER PER FISIOTERAPIA LASERIX PHP

    Device
    EU MDD · Eu Md Class 2b ·GN MED s.r.l.·On the market·1 country

    DOLORCLAST HIGH POWER LASER

    Device
    EU MDR · Eu Md Class 2b ·GN MED s.r.l.·On the market·32 countries

    LASERIX PRO SMART

    Device
    EU MDR · Eu Md Class 2b ·GN MED s.r.l.·On the market·3 countries

    LASERIX PRO

    Device
    EU MDR · Eu Md Class 2b ·GN MED s.r.l.·On the market·3 countries

    Laserix PRO

    Device
    EU MDD · Eu Md Class 2b ·GN MED s.r.l.·On the market·3 countries

    Laserix PH10

    Device
    EU MDD · Eu Md Class 2b ·GN MED s.r.l.·On the market·1 country

    ARM DolorClast Laser

    Device
    EU MDR · Eu Md Class 1 ·GN MED s.r.l.·On the market·32 countries

    CoLumbo

    FDA 510(k)
    FDA Class 2 ·Radiology

    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

    FDA Pre-Market Approval
    FDA Class 3 ·Amplia MRI CRT-D, Amplia MRI Quad CRT-D, Brava CRT-D, Brava Quad CRT-D, Claria MRI CRT-D, Claria MRI Quad CRT-D,Compia M

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·Advisa DR IPG, Advisa DR MRI IPG, Advisa SR MRI IPG

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Aurora EV ICD

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Evera XT VR ICD, Mirro MRI DR ICD, Mirro MRI VR IC

    COULTER GEN-S SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Protégé RX Carotid Stent System; Protégé GPS Self-Expanding Peripheral Stent System

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·EverFlex Self-Expanding Peripheral Stent System

    Medline Industries, Inc.

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10195327236052·GEN LAPAROSCOPIC

    Medline Industries, Inc.

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10889942847976·GEN MINOR