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

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    XPERT CT/NG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Aequalis™ Adjustable Reversed

    FDA UDI
    TORNIER, INC.·00846832068241·

    Biplanar 2-Column Plate, 10-Hole, Right, PRS Phoenix

    FDA UDI
    I.T.S. GmbH·09120069817003·

    Cervical Interbody 17mm x 13.5mm x 10mm Packaging

    FDA UDI
    XENCO MEDICAL LLC·B064XM11217101·Cervical Interbody 17mm x 13.5mm x 10mm

    Diversatek Healthcare

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·M7831217100·Gastric Sump Tube, 10 French

    CancelleX™ 17mm x 13.5mm x 10mm Cervical Interbody

    FDA UDI
    XENCO MEDICAL LLC·B064XM3D31217101·

    eTRAX™ Needle

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436102534·Sterile needle, 12GA x 17cm with (7.6 tapered t...

    BELIFU

    FDA Adverse Event
    Injury ·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020

    LUXATEMP ULTRA /STAR

    FDA 510(k)
    FDA Class 2 ·Dental

    FULL AUTO TONOMETER MODEL TX-20

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 21, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 21, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 21, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 21, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 21, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 21, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 21, 2015

    CONFIRM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code MXC·January 13, 2014

    HARMONIC SCALPEL CURVED SHEARS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·May 21, 2013

    UNKNOWN DEPUY LARGE-TAPER HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 9, 2011