BEUDAMED
    20 results · 44ms · Sources: EU EUDAMED, US FDA

    Xenco6850 (NT) - CancelleX Porous Titanium Lumbar Interbody Device

    FDA registration
    Isomedix Operations, Inc·1 product·🇺🇸 United States

    CancelleX Porous Titanium Lumbar Interbody Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K120364

    FDA registration
    NINGBO XINWELL MEDICAL TECHNOLOGY CO., LTD.·1 product·🇨🇳 China

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517576279·CoRoent Ant TLIF Ti, 9x10x36mm 4°

    CETRA

    FDA UDI
    Orthofix US LLC·18257200120581·3-LEVEL PLATE ASSEMBLY, 64MM

    CARTRIDGE BLOOD SET

    FDA registration
    Vantive US Healthcare LLC·1 product·🇺🇸 United States

    Isomedix Operations, Inc

    FDA registration
    Isomedix Operations, Inc·1 product·🇺🇸 United States

    DORNIER MEDTECH GMBH

    FDA registration
    DORNIER MEDTECH GMBH·1 product·🇩🇪 Germany

    CARTRIDGE BLOOD SET

    FDA registration
    GAMBRO RENAL PRODUCTS S.A. DE C.V.·1 product·🇲🇽 Mexico

    Steritec Services, LLC

    FDA registration
    Steritec Services, LLC·1 product·🇺🇸 United States

    CARTRIDGE LOW WEIGHT LOWVOLUME

    FDA registration
    Sterigenics U.S., LLC·1 product·🇺🇸 United States

    Allosource1516 (SDB) - VersaWrap; Versawrap Tendon Protector

    FDA registration
    Synergy Health AST, LLC·1 product·🇺🇸 United States

    Viant Medical, Inc.

    FDA registration
    Viant Medical, Inc.·1 product·🇺🇸 United States

    SAGE SERVICES GROUP

    FDA registration
    SAGE SERVICES GROUP·1 product·🇺🇸 United States

    EXTRA PTA BALLOON CATHETER WITH EMBOLIC PROTECTION FEATURE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GAMBRO CARTRIDGE BLOOD SET LOW WEIGHT- LOW VOLUME, MODEL 003422-520

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

    VersaWrap Tendon Protector

    FDA UDI
    ALAFAIR BIOSCIENCES, INC·B454VTP22011·VersaWrap Tendon Protector (K160364) is indicat...

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

    FDA classification
    FDA Class 2 ·Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

    Catheter, Angioplasty, Peripheral, Transluminal

    FDA classification
    FDA Class 2 ·Catheter, Angioplasty, Peripheral, Transluminal