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

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    GC FUJICEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Disposable Exam Packs

    FDA UDI
    PRACTICON, INC.·00723896021613·Pre-Sterilized Packs containing Mouth mirrors a...

    Preat Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092163627·Biomet 3i Certain®-compatible 4.1mm Engaging Ve...

    Scanlan® PrepMARK

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159025408·PrepMARK Surgical Skin Marker, Gentian Violet, ...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092126417·3i Certain 4.1mm Engaging Verification Cylinder...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008675·PedFuse Respond, CNL, 9.0mm x 30mm

    RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IMPOAID

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD¿ SYRINGE ONLY SLIP TIP, NON-STERILE, BULK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·May 24, 2018

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·February 20, 2014

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·March 13, 2013

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 25, 2011

    GEMSTAR 7 THERAPY PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·February 19, 2008

    S-ROM M HEAD 36MM +6

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·February 11, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·February 11, 2013

    PINNACLE 100 ACET CUP 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code LPH·April 26, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·February 20, 2014

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. REG. # 8010379·Product code JDI·April 26, 2013

    CORAIL2 STD SIZE 9

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS REG. # 3003895575·Product code KWA·April 26, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. REG. # 8010379·Product code KWA·April 26, 2013