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

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    EM SA Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772813148·GENUMEDI PRO SILVER SIZE I

    Edge™ Diamond ND010-4EF Composite Needle

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002585·Diamond dental bur, reusable

    Mueller Nasal Sponges

    FDA UDI
    Mueller Sports Medicine, Inc.·00074676191218·NASAL SPONGES, 25 PACK

    Remedy

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215008208·

    LinkBio Instrument

    FDA UDI
    Link Bio Corp·00810022402986·Impactor Plate, Tibial Cone Extra Small

    Paxeon Remedy

    FDA UDI
    PAXEON RECONSTRUCTION LLC·08177570201211·Remedy Stem Size 12 High Offset

    OrthoMedFlex, LLC

    FDA UDI
    ORTHOMEDFLEX LLC·M7161111912010·Orion Stem, H/O (Lateralized), - Size 12

    Remedy Hip Stem

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215053338·

    STRAIGHT ABUTMENT, 4.2, 4.6, 5.0, 6.4, IMPLANT 6.0, IMPLANT 7.0, IMPLANT 8.0 MODEL: 002061, 002062, 002063, 002064,

    FDA 510(k)
    FDA Class 2 ·Dental

    C7 XR IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYRINGE 3ML LL 200 S/C

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 11, 2021

    SKYLON Stem

    FDA UDI
    AMPLITUDE SAS·03701089520560·

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 13, 2022

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 29, 2026

    RUSCH EQUIPLED BLADEMAC 4

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·July 6, 2020

    RUSCH EQUIPLED BLADEMAC 4

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·July 6, 2020

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 26, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 25, 2011

    PROLIEVE THERMODILATATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 26, 2008