BEUDAMED
    1,810 results · 28ms · Sources: EU EUDAMED, US FDA

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    HD-550 Video Endoscope System

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

    SYNTEC-TAICHUNG NON-STERILE BONE PLATE AND SCREW IMPLANTS, MODEL#'S 222020-248120, 240050-240980, 241130-246620, 4240420

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    24M - Class A & BBP 21 - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620206·24M - Class A & BBP 21 - Metal

    NA

    FDA UDI
    Stryker GmbH·00886385008790·Titanium Ankle Fusion Nail, Left

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694020855·FPS 2.0mm x 20mm Locking Screw

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694075206·FPS 2.0 x 20mm Locking Screw Sterile Qty 5

    PHOTON PHOTON PLUS

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

    JUSTWO MODEL TME-601 ROOT APEX LOCATOR

    FDA 510(k)
    FDA Unclassified ·Unknown

    640G INSULIN PUMP MMT-1711K

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·April 8, 2020

    TW DRILL 1.1X105MM 18MM STP

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HBE·March 31, 2021

    GORE-TEX SUTURE CV7

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NBY·October 31, 2008

    FLOLINK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FPA·August 19, 2011

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FRN·July 3, 2013

    NUCLEUS CI512 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·October 22, 2020

    TBD

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA S.R.L.·Product code KRH·September 20, 2020

    INOGEN X4 CRT-D

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIK·April 9, 2020

    INVACARE RELIANT 450 HOYER LIFT

    FDA Adverse Event
    Malfunction ·INVACARE CORPORATION (TW)·Product code FSA·March 31, 2021

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·January 22, 2020

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·January 22, 2020

    NUCLEUS 22

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·December 21, 2020