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

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    ENDOGRAPH DC

    FDA 510(k)
    FDA Class 2 ·Dental

    GYRUS ACMI, INC

    FDA UDI
    Gyrus ACMI, LLC·00821925011847·HOUGH PICK LARGE CURVE 12.7 MM TIP LENGTH STAIN...

    ArgenZ HT+ 98x16 A1B

    FDA UDI
    ARGEN CORPORATION, THE·D818130109·Dental porcelain/ceramic restoration kit

    AF811

    FDA UDI
    Respironics, Inc.·00606959042407·Philips Procedure, AF811 with Filtered Exhalati...

    MotoBAND

    FDA UDI
    CROSSROADS EXTREMITY SYSTEMS·00815432022120·The MotoBAND™ CP Implant System is a bone plati...

    Tecno

    FDA UDI
    TECNO INSTRUMENTS (PVT) LTD·08964003293192·Cusco Vaginal Speculum (Medium)

    SPLINTER FORCEPS LOWER

    FDA UDI
    W.H. Holden, Inc.·D9281301090·

    LOGIFLEX LAPAROSCOPIC BAND POSITIONING DEVICE

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

    ELECTROPHYSIOLOGY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REAMER SHAFT, MOD, TRINKLE 8.0X284 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWE·February 13, 2012

    ULTICARE

    FDA Adverse Event
    Other ·ULTIMED, INC·Product code FMI·May 10, 2013

    INSPIRE 7F M N/S

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·December 29, 2025

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 24, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 18, 2014

    CONCERTO CRT-D DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NIK·June 16, 2011

    INSPIRE 7F M N/S

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA - S.R.L.·Product code DTZ·February 19, 2026

    HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHELL VENOUS/CAR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 10, 2019

    INSPIRE 6F HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code DTZ·March 10, 2017

    INSPIRE 6F HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·August 3, 2022

    INSPIRE 6 HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·February 25, 2022