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

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    NEONATALIE RESUSCITATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NexxZr™ T / D-100-22-NT-D400-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271113825·

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981201005·Interbody, 11mm x 32mm x 17mm, 20 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981208127·Trial, 11mm x 32mm x 17mm, 20 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981193010·Interbody, 11mm x 32mm x 17mm, 20 deg

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973875·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973790·

    MSA HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DISPOSABLE POWDER FREE VINYL EXAM GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PROSTAR

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·August 22, 2024

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code FSA·October 1, 2014

    ACCU-CHEK ® SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·May 29, 2013

    INRATIO

    FDA Adverse Event
    Other ·ALERE SAN DIEGO, INC.·Product code GJS·June 3, 2011

    LUNA Chest, Model No. LU4006

    FDA Enforcement
    Class III ·Terminated·Novadaq Technologies, Inc.·December 3, 2014