BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    Vial Adapter Ø20 mm

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ophthalmic Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101100·HELVESTON "GREAT BIG BARBIE" RETRACTOR 11MM

    Pre-Finisher

    FDA UDI
    TP ORTHODONTICS INC·00192029041727·Non-Extraction w/Seating Springs

    U2 HIP SYSTEM, EXPANDED INDICATIONS FOR USE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SKYRON INTEGRITY 215 STEAM STERILIZER SKYTRON INTEGRITY 215 SG STEAM STERILIZER SAKURA STEAM STERILIZER ASSV-AB09 SAKURA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    QUADROX-ID

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·October 17, 2014

    AVEA

    FDA Adverse Event
    Malfunction ·CAREFUSION 207, INC.·Product code CBK·August 1, 2011

    PERFORMA DIANGONSTIC CARDIOLOGY CATHETER

    FDA Adverse Event
    Injury ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·June 21, 2013

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 29, 2025

    GMK-REVISION TIBIAL AUGMENTATION SIZE 2/10MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·June 23, 2023

    GMK-HINGE FEMORAL COMPONENT SIZE 2 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·February 7, 2022

    GMK-REVISION FIXED TIBIAL TRAY CEMENTED SIZE 3 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 29, 2019

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 4/10MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 4, 2019