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

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    Everest Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POUR-PLUS

    FDA UDI
    Denplus Inc·D8451151216·POUR-PLUS, ORI, 2.3 kg

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169502161·INTERBODY 2151216 MEDIUM - 6 DEG 16MM

    PRECICE® INTRAMEDULLARY LIMB LENGTHENING ROD

    FDA Adverse Event
    Injury ·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code HSB·June 28, 2016

    TALOS®-A

    FDA UDI
    SpineArt SA·07640375237958·TALOS®-A (HA) PEEK PLANAR, SYMMETRIC IBFD D28 ...

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321512160·

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295043010·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM 16X80MM

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575291281·Orthopaedic implant aiming/guiding block, reusa...

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295043027·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM 16X130MM

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575291304·Orthopaedic implant aiming/guiding block, reusa...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575291342·Orthopaedic implant aiming/guiding block, reusa...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575291328·Orthopaedic implant aiming/guiding block, reusa...

    AUDIT MICROCV PROTEIN LINEARITY SET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    HYDRALOK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HAMILTON-C1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·August 30, 2024

    PHILIPS SONICARE

    FDA Adverse Event
    Injury ·PHILIPS ORAL HEALTHCARE·Product code JEQ·July 19, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·June 30, 2011

    DAMON COPPER NITI WIRE

    FDA Adverse Event
    Malfunction ·ORMCO CORPORATION·Product code DZC·September 9, 2008

    ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty Part Number: 1512-16-080

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code JWH·July 1, 2021