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

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    Filters Regulation: Us FDA ×

    GENESYS SPINE ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MOBIS XL 0°

    FDA UDI
    SIGNUS Medizintechnik GmbH·04047844001691·The KIMBA®, KIMBA® mini, MOBIS® and NOVAL™ impl...

    NA

    FDA UDI
    Smith & Nephew, Inc.·03596010037862·ANGLED STAPLE DRIVER-EXTRACTOR

    Axiom®

    FDA UDI
    AXIOM MEDICAL, INCORPORATED·M6651111320·Thoracic Catheter, Right Angle, Silicone

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08806390852418·

    RINGLOC INSTRUMENTATION

    FDA UDI
    Biomet Uk Ltd·05019279414925·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587P11113270·11mm PLIF Implant 11mm Wide 32mm Length, 7 deg ...

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089436040·

    AIRLIFE HEPA FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, (BLUE, WHITE, PINK)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HIP BALL BIOLOX 32 +5 12/14

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 12, 2022

    HIP BALL BIOLOX 32 +5 12/14

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LPH·February 10, 2026

    BD PLASTIPAK¿ - 3-PIECE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 28, 2022

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 14, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 23, 2014

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code MIH·May 25, 2011

    HIP BALL BIOLOX 32 +5 12/14

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·December 22, 2021

    HIP BALL BIOLOX 32 +5 12/14

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code LPH·July 12, 2024

    5.5 EXP VERSE UNITIZED SET SCR

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code NKB·December 19, 2019

    5.5 EXP VERSE SCR 6.0X45

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL CH·Product code NKB·December 19, 2019