BEUDAMED
    23 results · 33ms · Sources: EU EUDAMED, US FDA

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    DEPILASE TWIN LASE LASER SYSTEM

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

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·37613154184171·Bone Screws, Cross-Pin

    APC™ II Unitek™ Mini Uni-Twin

    FDA UDI
    3M UNITEK CORPORATION·00652221061676·Mini Uni-Twin(TM) Bracket APC(TM) II Standard E...

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717104077·Stainless Steel K Files (Hand), Size # 08, Leng...

    APC™ PLUS Unitek™ Mini Uni-Twin

    FDA UDI
    3M UNITEK CORPORATION·00652221092694·Mini Uni-Twin(TM) Bracket APC(TM) PLUS Standard...

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113232·PS Insert, Size 4 x 12mm

    FLEXIBLE ENDOSCOPIC SCISSORS

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

    VISION R/F TILTING TABLE

    FDA 510(k)
    FDA Class 2 ·Radiology

    BONE SCREWS, CROSS-PIN, DIAM.2.0X12MM, (5/PACKAGE)

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code JEY·March 24, 2016

    BONE SCREWS, CROSS-PIN, DIAM.2.0X12MM, (5/PACKAGE)

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code JEY·March 30, 2016

    DEROYAL GENERAL PURPOSE PROBE 12FR

    FDA Adverse Event
    Injury ·DEROYAL CIENTIFICA DE LATINOAMERICA S.R.L.·Product code FLL·April 22, 2016

    BONE SCREWS, CROSS-PIN, DIAM.2.0X12MM, (5/PACKAGE)

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code JEY·January 30, 2017

    MINI PLATE, 4-HOLES, WITH BAR (1/P)

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code JEY·September 22, 2010

    DEROYAL GENERAL PURPOSE PROBE 12FR

    FDA Adverse Event
    Malfunction ·DEROYAL CIENTIFICA DE LATINOAMAERICA S.R.L.·Product code FLL·April 15, 2016

    PRIMARY MANDIBULAR RECONSTRUCTION PLATE, 11-HOLES, WITH TEMPLATE

    FDA Adverse Event
    Injury ·STRYKER LEIBINGER FREIBURG·Product code JEY·June 15, 2022

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code LFR·May 31, 2007

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013

    TRILOGY ALTERNATE BEARING SHELL INSERT

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code MRA·February 8, 2011

    BONE SCREWS, CROSS-PIN, DIAM.2.0X12MM, (5/PACKAGE)

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code JEY·July 1, 2016

    KING LAD Standard ClearSeal SINGLE USE, King Systems ETO Sterilie, 10 devices/case Size 4 / Adult ClearSeal King LAD¿ Patient Size: 50-70kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012