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

    None

    FDA registration
    Amphenol Cable and Interconnect Technologies Asia Pacific Ltd.·1 product·🇭🇰 Hong Kong

    None

    FDA registration
    Amphenol Medical Technologies (Dongguan) Co., Ltd.·1 product·🇨🇳 China

    Eclipse PRO cable P/N 700-0372-01 700-0373-01 700-3878-01 700-0374-01 700-0375-01 700-0376-01 700-0379-01 700-0377-01

    FDA registration
    Spacelabs Healthcare Inc.·1 product·🇺🇸 United States

    Eclipse PRO cable P/N 700-0372-01 700-0373-01 700-3878-01 700-0374-01 700-0375-01 700-0376-01 700-0379-01 700-0377-01

    FDA registration
    SPACELABS HEALTHCARE LTD.·1 product·🇬🇧 United Kingdom

    Eclipse PRO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Electrocardiograph, Ambulatory (Without Analysis)

    FDA classification
    FDA Class 2 ·Electrocardiograph, Ambulatory (Without Analysis)

    Isomedix Operations, Inc.

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

    ORTHOLOC 3Di Foot Reconstruction System

    FDA registration
    WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

    ORTHOLOC 3DI Midfoot/Flatfoot System

    FDA registration
    HG Medical GmbH·1 product·🇩🇪 Germany

    Apex (Guangzhou) Tools & Orthopedics Company

    FDA registration
    Apex (Guangzhou) Tools & Orthopedics Company·1 product·🇨🇳 China

    MEDICAL COMPONENTS INC

    FDA registration
    MEDICAL COMPONENTS INC·1 product·🇺🇸 United States

    ORTHOLOC 3Di Foot Reconstruction System

    FDA registration
    WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

    MEDCOMP SPLIT CATH III (CARBOTHANE)

    FDA registration
    Cosmed Group, Inc., d/b/a Cosmed of NJ·1 product·🇺🇸 United States

    Kit, Box of 20 PMSENS71-P INVOS™ Pediatric rSO2 Sensor

    FDA registration
    CELESTICA ELECTRONICS (S) PTE LTD.·2 products·🇸🇬 Singapore

    GI Genius

    FDA registration
    LINKVERSE S.R.L.·1 product·🇮🇹 Italy

    Penumbra System (Reperfusion Catheters, Separators, Aspiration Tubing, and 3D Revascularization Device)

    FDA registration
    Sterigenics US LLC·1 product·🇺🇸 United States

    ORTHOLOC 3DI MIDFOOT/FLATFOOT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPLIT CATH III

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

    Catheter, Hemodialysis, Implanted

    FDA classification
    FDA Class 2 ·Catheter, Hemodialysis, Implanted

    Plate, Fixation, Bone

    FDA classification
    FDA Class 2 ·Plate, Fixation, Bone