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

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    THERMAL CAUTERY UNIT, MODEL 150

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NA

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490027878·VENT TUBE 1002341 5PK V-T 1.27 C-FLEX

    C-Flex®

    FDA UDI
    MEDTRONIC XOMED, INC.·00763000281854·VENT TUBE 1002341 5PK V-T 1.27 C-FLEX

    DR5000 DEDICATED CHEST X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    WILLI GELLER CREATION & AV PORCELAIN

    FDA 510(k)
    FDA Class 2 ·Dental

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 25, 2013

    INTELLIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 14, 2025

    DREAMSTATION CPAP

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·January 6, 2022

    RUSCH GREENLITE DISP MTL MAC 4

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·July 13, 2020

    RUSCH GREENLITE DISP MTL MAC 4

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·May 5, 2020

    RUSCH GREENLITE DISP MTL MAC 4

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·July 10, 2020

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·March 13, 2013

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

    EXTERNAL PATIENT RECHARGER SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·February 22, 2008

    45 MM LEFT STANDARD MANDIBLE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 8, 2014

    VANTA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 5, 2021

    ACETABULAR CUP HAP SIZE 52/58

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·July 10, 2020

    45 MM RIGHT STANDARD MANDIBLE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·August 8, 2014

    TMJ SYSTEM CROSS DRIVE EMERGENCY FOSSA SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·May 3, 2018

    "2.4MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·May 3, 2018