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

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    SMILIE PC

    FDA 510(k)
    FDA Class 1 ·Dental

    Preat Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092179291·Straumann BL RC-compatible Scan Body Kit Contai...

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489105657·PowerChem Neoprene Exam Gloves, Extra Large

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00141451·

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001445·artVeneer life upper anteriors, IS, D2

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008484·PedFuse Respond, CNL, 7.0mm x 45mm

    BIPAP HARMONY S/T, MODEL 1001445

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MEDTRONIC MODEL 7499 EXTENSION

    FDA 510(k)
    FDA Class 2 ·Neurology

    SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-6000

    FDA 510(k)
    FDA Class 2 ·Hematology

    DELTA CER HEAD 12/14 32MM +1

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code LZO·March 13, 2013

    SM BONE FASTAK, TAPERED NEEDLE W/#2-0 FIBERWIRE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·February 25, 2011

    ADVANCED VENOUS ACCESS CATHETER

    FDA Adverse Event
    Other ·EDWARDS LIFESCIENCES, PR·Product code DQO·February 14, 2008

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 9, 2019

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Death ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 8, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 9, 2019

    TMJ SYSTEM RIGHT FOSSA COMPONENT, SMALL

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·March 26, 2018

    TMJ SYSTEM RIGHT STANDARD MANDIBULAR COMPONENT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·March 26, 2018

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Death ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JWH·October 8, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Death ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 8, 2019

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 9, 2019