BEUDAMED
    402 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    VASCUCLEAR PRECISION BIPOLAR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Recon

    FDA UDI
    Revelation Medical Devices·G3181029830·Skid Shoehorn Retractor

    C.T.M. POWER CHAIR, MODEL HS-5600

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ACIST 4 FRENCH ANGIOGRAPHIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·March 29, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·May 27, 2021

    2520274-2013-02482

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·May 9, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·May 25, 2011

    COMPANION 1000

    FDA Adverse Event
    Death ·PLAINFIELD-LOX-RX·Product code BYJ·August 8, 2008

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 6, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·March 24, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·June 15, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·May 18, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·June 7, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 2, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 8, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 16, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 28, 2021

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·Product code MNT·November 24, 2020

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·July 2, 2021