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

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    CLEO PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550131·GENUMEDI PT KNEE SUP SILVER L EW IV

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814213·GENUMEDI PT SILVER L IV

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694009072·2 x 4 Hole Oblique Right Compression T Plate

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·November 29, 2018

    RELIANCE ENDOSCOPE PROCESSING SYSTEM

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

    BONE-LOK MVP CORTICAL-CANCELLOUS COMPRESSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 29, 2013

    ASPEN

    FDA Adverse Event
    Malfunction ·*·Product code KCY·June 9, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    VARIABLE SELF-DRILLING SCREW DIAM. 4X14MM (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·October 4, 2017

    Microtek Franz Angiography Drape with Radiation Shield, Item # RBA202, and Microtek Angiography Drape with Radiation Shield and Pouches, Item # RBA203. Sterile EO. Microtek Medical, Inc., Columbus, MS 39702.

    FDA Enforcement
    Class II ·Terminated·Ecolab Inc·September 14, 2016