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

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    SKINTEMP II

    FDA 510(k)
    FDA Unclassified ·Unknown

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517636577·CoRoent Ant TLIF PEEK, 12x12x32mm 15°

    JOBST UltraSheer

    FDA UDI
    BSN MEDICAL, INC.·00035664223250·ULTRA SHEER 30-40 MM HG THIGH W/DOT BAND CLOSED...

    Bernafon

    FDA UDI
    Bernafon AG·05711584022801·MD3 NR, PS MAC MONDO 3

    Lateral Hydrodissection Cannula, 25ga

    FDA UDI
    KATALYST SURGICAL LLC·00840096205640·Lateral Hydrodissection Cannula, 25ga

    DANmed

    FDA UDI
    DANNORITZER Medizintechnik GmbH & Co. KG·04251351108426·LAP-Instrument, Ø5mm, l=250mm, flushp. Graspi...

    DANmed

    FDA UDI
    DANNORITZER Medizintechnik GmbH & Co. KG·04251351102202·LAP-Instrument, Ø5mm, l=250mm, flushp. Graspi...

    DANmed

    FDA UDI
    DANNORITZER Medizintechnik GmbH & Co. KG·04251351112157·LAP-Instrument, Ø5mm, l=250mm, detach. Graspi...

    DANmed

    FDA UDI
    DANNORITZER Medizintechnik GmbH & Co. KG·04251351110290·LAP-Instrument, Ø5mm, l=250mm, detach. Graspi...

    DANmed

    FDA UDI
    DANNORITZER Medizintechnik GmbH & Co. KG·04251351104381·LAP-Instrument, Ø5mm, l=250mm, detach. Graspi...

    DANmed

    FDA UDI
    DANNORITZER Medizintechnik GmbH & Co. KG·04251351117008·LAP-Insert only, Ø5mm, l=250mm Graspi...

    DANmed

    FDA UDI
    DANNORITZER Medizintechnik GmbH & Co. KG·04251351114755·LAP-Instrument, Ø5mm, l=250mm, detach. Graspi...

    NORMED TITANIUM OSTEOTOMY PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IDRIVE SYSTEM (I DRIVE POWER HANDLE, IDRIVE (RALC) SINGLE USE RELOAD)

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

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970508·

    LINOX SMART SD 65/18

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVY·May 21, 2013

    UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·June 13, 2011

    HEARTSTREAM XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·August 15, 2008

    BD EMERALD¿ 2ML SYRINGE, LUER SLIP CENTRIC TIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 6, 2017

    UNITIP CATHETER FOR HR GI

    FDA Adverse Event
    Malfunction ·UNISENSOR USA INC·Product code FFX·January 16, 2015