BEUDAMED
    274 results · 23ms · Sources: EU EUDAMED, US FDA

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    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEL 80 EXCIMER LASER SYSTEM

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEL 90 EXCIMER LASER SYSTEM

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEL90

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEL 90 Excimer Laser

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEL 80 EXCIMER LASER SYSTEM

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEL 80 Excimer Laser

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEL 80 Excimer Laser System

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEDITEC MEL 80 EXCIMER LASER SYSTEM

    Excimer Laser System

    FDA Pre-Market Approval
    FDA Class 3 ·MEL 80 Excimer Laser System

    HI-TORQUE COMMAND™

    FDA UDI
    ABBOTT VASCULAR INC.·08717648356872·HI-TORQUE COMMAND™ 14 MT Guide Wire with Hydrop...

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481125324·Locator F-Tx Abutment for 3.0 Internal Hex Conn...

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481116056·LOCATOR R-Tx Abutment for 3.0 Internal Hex Conn...

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481129056·LOCATOR R-Tx Abutment, 3.0mm Internal Hex Conne...

    Baby Gorilla/Gorilla Plating System

    FDA UDI
    Paragon 28, Inc.·00889795049094·Gorilla, Ankle Fx, Medial Malleolus Plate, Hook...

    3cc Citregraft Cylinder

    FDA UDI
    Acuitive Technologies, Inc.·00810027272294·3cc Citregraft Cylinder

    CALDERA MESH

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

    CTC VASOPRESS COMPRESSION SLEEVES

    FDA Adverse Event
    Injury ·CTC COMPRESSION THERAPY CONCEPTS·Product code JOW·April 11, 2013

    ACUITY

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·April 15, 2011

    PROTEUS XR/A

    FDA Adverse Event
    Malfunction ·GE HANGWEI MEDICAL SYSTEMS, CO., LTD.·Product code KPR·June 11, 2008

    The Model 8540 Catheter Access Port Kit is intended for use in accessing the catheter via the catheter access port of Medtronic(R) implantable programmable infusion pumps (except Medtronic MiniMed pumps). The Model 8540 Catheter Access Port Kit does not have a product code for itself; it is approved under PMA P860004. PMA P860004 is classified as: pump, infusion, implanted, programmable under product code LKK.

    FDA Recall
    Terminated ·Medtronic Inc, Neurological & Spinal Division·Product code LKK·July 23, 2004