BEUDAMED
    10,000 results · 48ms · Sources: EU EUDAMED, US FDA

    Sensitiv Imago Model 135

    FDA registration
    ALFA-MED LLC·1 product·🇷🇺 Russian Federation

    OXIDAR

    FDA registration
    INDUSTRIAS PLASTICAS MEDICAS, S.A. DE C.V.·1 product·🇲🇽 Mexico

    IPM

    FDA registration
    INDUSTRIAS PLASTICAS MEDICAS, S.A. DE C.V.·1 product·🇲🇽 Mexico

    CISTODREN

    FDA registration
    INDUSTRIAS PLASTICAS MEDICAS, S.A. DE C.V.·1 product·🇲🇽 Mexico

    CISTODREN

    FDA registration
    INDUSTRIAS PLASTICAS MEDICAS, S.A. DE C.V.·1 product·🇲🇽 Mexico

    IPM

    FDA registration
    INDUSTRIAS PLASTICAS MEDICAS, S.A. DE C.V.·1 product·🇲🇽 Mexico

    IPM

    FDA registration
    INDUSTRIAS PLASTICAS MEDICAS, S.A. DE C.V.·1 product·🇲🇽 Mexico

    PHILIPS

    FDA UDI
    Respironics California, Inc.·00884838015920·Cfgkit,V60,NIST/Boc,Wht,Fm,Cord:UK

    AOC, OSTENE, AOC IMPLANT MATERIAL, CERETENE, OSTENE LUBE, AOC-LV

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    VU GIA DENTAL LAB CO., LTD.

    FDA registration
    VU GIA DENTAL LAB CO., LTD.·1 product·🇻🇳 Vietnam

    VU GIA DENTAL LAB CO., LTD.

    FDA registration
    VU GIA DENTAL LAB CO., LTD.·1 product·🇻🇳 Vietnam

    VU GIA DENTAL LAB CO., LTD.

    FDA registration
    VU GIA DENTAL LAB CO., LTD.·1 product·🇻🇳 Vietnam

    VU GIA DENTAL LAB CO., LTD.

    FDA registration
    VU GIA DENTAL LAB CO., LTD.·1 product·🇻🇳 Vietnam

    VIALMIX®RFID

    FDA UDI
    LANTHEUS MEDICAL IMAGING, INC.·00866709000402·Class I medical device, Amalgamator, Dental, AC...

    BRANCH MY NGUYEN MANUFACTURING CO., LTD.

    FDA registration
    BRANCH MY NGUYEN MANUFACTURING CO., LTD.·1 product·🇻🇳 Vietnam

    PRONTO DOC

    Device
    EU MDD · Eu Md Class 2a ·Eurosirel Spa·On the market·1 country

    AOC POROUS POLYETHYLENE, AOC POROUS HDPE, AOC POROUS POLYETHYLENE SURGICAL IMPLANT

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

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·DIVA PLATFORM,DERMA PLATFORM

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

    FDA Pre-Market Approval
    FDA Class 3 ·INSYNC ICD 7272

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·GEM III DR 7275, GEM III VR 7231, GEM DR 7271