BEUDAMED
    912 results · 22ms · 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 ×

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K1220100·Breaker, Extended Tab

    Z6 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Likorall™ overhead lift

    FDA UDI
    Liko AB·00887761979819·Overhead track patient lifting/transfer system

    MONOPTY

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741084669·MONOPTY® Disposable Core Biopsy Instrument, 22m...

    ArgenZ HT+ 98x14 A1-L

    FDA UDI
    ARGEN CORPORATION, THE·D818122010·Dental porcelain/ceramic restoration kit

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193110073·HA PEEK EVOS Straight, ,10mmx9mmx 22mm , BICONV...

    36M - Class B 21 White Cap - 36 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588220109·36M - Class B 21 White Cap - 36 Metal

    36M - Class B 21 White Cap - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620107·36M - Class B 21 White Cap - Metal

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981246556·Interbody, 39mm x 27mm X 20mm, 10 Deg

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981265809·Trial, 39mm x 27mm x 20mm, 10 deg

    VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TOTAL KNEE FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIEGO CONSOLE TRIGGER ENABLED

    FDA Adverse Event
    Injury ·GYRUS ACMI, INC.·Product code ERL·May 16, 2013

    MIRA-I CS RETRACTOR BODY

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·September 19, 2014

    TM REVERSE GLENOSPHERE DISTRACTOR

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HWB·May 24, 2011

    AVALON FM50 FETAL MONITOR

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code HGM·March 1, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·December 8, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD./HUNTINGTON·Product code MFK·July 30, 2010

    COSGROVE-EDWARDS TRICUSPID ANNULOPLASTY SYSTEM WITH DURAFLO TREATMENT

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code KRH·June 2, 2010

    SYBRONPRO TL

    FDA Adverse Event
    Injury ·EBI INC.·Product code DZE·June 11, 2010