BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    LIQUI-SERA COMBO LIGAND/TDM CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    FREEDOM

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ACTH RIA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 10, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 10, 2012

    UNIFY ASSURA CRT-D RF HV

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NIK·June 23, 2015

    MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01

    FDA Recall
    Open, Classified ·Unetixs Vascular, Inc.·Product code JAF·February 10, 2023

    MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01

    FDA Recall
    Open, Classified ·Unetixs Vascular, Inc.·Product code JAF·February 10, 2023

    MultiLab Series II REVO non-invasive vascular diagnostic device, Model Number 12950-0000-01

    FDA Recall
    Open, Classified ·Unetixs Vascular, Inc.·Product code JAF·February 10, 2023

    MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device, Model Number 11996-0000-01

    FDA Recall
    Open, Classified ·Unetixs Vascular, Inc.·Product code JAF·February 10, 2023