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

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    SNAP WOUND CARE SYSTEM

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

    RC Cem. Abutment

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600306139·

    NexxZr™ T / D-100-14-NT-B300-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271112903·

    Forestanit®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR21320801·Forestanit wire round spring-hard laboratory co...

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981207786·Trial, 11mm x 32mm x 8mm, 0 deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981200664·Interbody, 11mm x 32mm x 8mm, 0 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981192679·Interbody, 11mm x 32mm x 8mm, 0 deg

    DEPUY RECLAIM REVISION HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROSTAM LTD FRAGRANCED PLASTIC APPLICATOR TAMPONS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    EZ STEER¿ THERMOCOOL® NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Death ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code OAD·June 16, 2011

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 15, 2024

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 22, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

    METACROSS OTW PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019