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

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    Filters Regulation: Us FDA ×

    CS 9600

    FDA 510(k)
    FDA Class 2 ·Radiology

    Vilex Jones Fracture Guidewire

    FDA UDI
    VILEX LLC·00841731123558·Wire, Guide 1.8x200mm Sgl Trocar

    Lapiplasty SpeedPlate

    FDA UDI
    Treace Medical Concepts, Inc.·00810111222600·Inserter Rod

    MICRO FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896084636·MICRO FORCEPS CURVED TUNGSTEN CARBIDE DUST TIP ...

    n/a

    FDA UDI
    HANS RUDOLPH, INC.·00874750007325·2700 2WAY LG TSHP SUB ASSY

    Initia Total Hip System

    FDA UDI
    KYOCERA CORPORATION·04547898306402·STD LINER 40-66/70

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306805141·Neivert Osteotome, Curved, Right, 20cm

    DESS dental smart solutions

    FDA UDI
    TERRATS MEDICAL SL.·08435457200390·Conical BL

    Carnegie Surgical LLC

    FDA UDI
    Carnegie Surgical LLC·G1412001830·Neivert Osteotome - Curved, Right: 20cm/8 Inch

    PISCES PLUS (DW286 C)

    FDA 510(k)
    FDA Class 2 ·Dental

    HARDYDISK, PIPERACILLIN, 100MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    COMPASSIONATE USE DEVICE

    FDA Adverse Event
    Injury ·3D SYSTEMS·Product code PBF·November 11, 2020

    FEMORAL MODULAR HEAD - M 28MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·May 20, 2021

    SMR SYSTEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code KWT·March 26, 2026

    TECNIS CL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·October 24, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

    UNK

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·July 1, 2013

    INSPIRE 7F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·September 15, 2022

    INSPIRE 7F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL.·Product code DTZ·March 12, 2024

    INSPIRE 7F

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·June 24, 2025