BEUDAMED
    24 results · 22ms · Sources: EU EUDAMED, US FDA

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    CLEVER TD-7001NEBULIZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1220600·12mm H x 20mm W x 60mm L x 0 degrees XLIF

    Class A BMD 21 - 16 Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620602·Class A BMD 21 - 16 Poly White

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741220600·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X122060120·12mm H x 20mm W x 60mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X12206080·12mm H x 20mm L x 60mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L122060120·12mm H x 20mm W x 60mm L XLIF Trial 12 degree L...

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K1220100·Breaker, Extended Tab

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674122060060·

    LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES

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

    RADIANCE

    FDA 510(k)
    FDA Class 2 ·Radiology

    EZ STEER¿ THERMOCOOL® NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·February 22, 2012

    LASSO¿ ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DRF·February 22, 2012

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 19, 2025

    COMP RVS TRAY CO 44MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code KWS·July 21, 2017

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    DEPUY ASR XL FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 21, 2013

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 26, 2014

    DLT TS CER HD 12/14 32MM +9

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIV. OF DEPUY ORTHOPAEDICS·Product code LZO·June 3, 2011

    LIFEPAK® 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019