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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Flat Panel Detector

    FDA 510(k)
    FDA Class 2 ·Radiology

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221714150·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221714000·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221714070·

    BD BBL™ Todd Hewitt Broth

    FDA UDI
    BECTON, DICKINSON AND COMPANY·30382902217146·BD BBL™ Todd Hewitt Broth, 5 mL, Carton of 100 ...

    STILLE Raspatories

    FDA UDI
    Stille AB·07332339207243·RASPATORY WIBERG STILLE straight 4 mm 17 cm 6.7...

    CAPTURE-R READY-SCREEN (3)

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·October 26, 2016

    SMITH & NEPHEW, INC. SHOULDER SYSTEM INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RT-PLUS PE INSERT CLAMP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·November 3, 2014

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·August 15, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·July 11, 2013