BEUDAMED
    184 results · 21ms · Sources: EU EUDAMED, US FDA

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    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·OSTEOSPACE

    Atos Medical

    FDA UDI
    ATOS MEDICAL INC.·00817126020658·2010-058 Laryngectomy Pulmonary Kit 9/55 With P...

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828111560·GEN4 DIGITAL

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828109253·GEN4 DIGITAL

    Plastic Cylinder with Hex Ti

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118141693·Plastic Cylinder with Hex Ti

    Plastic Cylinder with Hex Ti

    FDA UDI
    T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10810190011215·

    NA

    FDA UDI
    STRYKER CORPORATION·07613327175288·Restraint Strap

    IMAGE IV DICOM IMAGE ARCHIVAL PACS NETWORK

    FDA 510(k)
    FDA Class 2 ·Radiology

    Electrosurgical, Radio Frequency, Refractive Correction

    FDA Pre-Market Approval
    FDA Class 3 ·VIEWPOINT(TM) CK SYSTEM

    Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·June 14, 2013

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·July 26, 2012

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·July 26, 2012

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 24, 2012

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code MCX·March 8, 2011

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·June 14, 2013

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·February 5, 2014

    INDUCTOS

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·October 5, 2011