BEUDAMED
    10,000 results · 39ms · 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 ×

    R+

    FDA UDI
    ALLWIN MEDICAL DEVICES, INC.·00812261011882·R+ Urinary Diversion Stents [Mono - J] Open Tip...

    4.0MM TI CANCELLOUS POLYAXIAL SCREW 18MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWP·October 23, 2014

    TERUMO OVERPRESSURE SAFETY VALVE

    FDA Adverse Event
    Injury ·*·Product code MNJ·February 5, 2009

    MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PERFUSION SYSTEMS·Product code MNJ·March 4, 2004

    MEDTRONIC VRV-100

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOPULMONARY-ANAHEIM·Product code MNJ·April 3, 2000

    MEDTRONIC VRV-100

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOPULMONARY- ANAHEIM·Product code MNJ·April 12, 2000

    MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PERFUSION SYSTEMS·Product code MNJ·July 6, 2004

    PRESSURE REDUCTION VALVE

    FDA Adverse Event
    Malfunction ·LINDE AG·Product code MNJ·April 9, 1999

    BARD OPS VALVE

    FDA Adverse Event
    Injury ·BARD VASCULAR SYSTEM·Product code MNJ·June 23, 1999

    9610614-1999-00002

    FDA Adverse Event
    Other ·Product code MNJ·April 9, 1999

    VRV-II (STERILE)

    FDA Adverse Event
    Injury ·QUEST MEDICAL, INC.·Product code MNJ·July 30, 1998

    VRV-II (NON-STERILE)

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC.·Product code MNJ·July 20, 1998

    OVER PRESSURE VALVE

    FDA Adverse Event
    Malfunction ·BARD VASCULAR SYSTEM·Product code MNJ·October 31, 1996

    MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PERFUSION SYSTEMS·Product code MNJ·March 29, 2006

    VACUUM RELIEF VALVE IIC-CLEAR

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC.·Product code MNJ·May 16, 2006

    MEDTRONIC OVERPRESSURE/VACUUM RELIEF VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PERFUSION SYSTEMS·Product code MNJ·April 3, 2006

    2021710-2001-00147

    FDA Adverse Event
    Malfunction ·Product code MNJ·November 6, 2001

    VACUUM RELIEF VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PERFUSION SYSTEMS·Product code MNJ·December 26, 2001

    BIRD

    FDA Adverse Event
    Injury ·BIRD PRODUCTS CORP.·Product code MNJ·November 6, 2001

    *

    FDA Adverse Event
    Malfunction ·BIRD PRODUCTS CORP.·Product code MNJ·November 6, 2001