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

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    Selectra Catheters, Selectra Accessory Kit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Padded Arm Sling

    FDA UDI
    MEDICAL SPECIALTIES INCORPORATED·00802357832651·

    MobileLink Acetabular Cup System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575176854·Standard UHMWPE Insert - shouldered 5 mm

    MobileLink Acetabular Cup System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575176861·Standard UHMWPE Insert - shouldered 5 mm

    JAZZ WIRELESS BLOOD GLUCOSE MONITORING SYSTEM, MODEL 8000-03381

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NHANES WHOLE BODY DXA REFERENCE DATABASE

    FDA 510(k)
    FDA Class 2 ·Radiology

    TUBE SET FOR SUCTION SINGLE-USE

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·December 2, 2019

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 17, 2014

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 21, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·August 7, 2013