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

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    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0310030·Probe, 1.5 inch Ball, Steffee, Curved, Black

    STIMULUS/DISSECTION INSTRUMENTS, BALL-TIP PROBES

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ACRY FORM

    FDA UDI
    DENTAL MANUFACTURING SPA·08056865003139·

    Humeral Cup Stability

    FDA UDI
    FX SOLUTIONS·03701037309414·HUMERAL CUP STABILITY PE/TA6V Ø36/+3

    NA

    FDA UDI
    Stryker GmbH·00886385024295·Screwdriver handle, AO

    Humeral Cup Stability

    FDA UDI
    FX SOLUTIONS·03701037307885·STABILITY TRIAL CUP Ø36 +3

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930703100300·Bed Attachment One Hole

    TRANSDUCER, S8-3T MICRO TEE

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND, INC.·Product code IYO·August 8, 2014

    SAFESTING AND SAFESTING HUB

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Z-NET

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TRANSDUCER, S8-3T MICRO TEE

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND, INC.·Product code IYO·March 28, 2014

    TRANSDUCER, S8 3T MICRO TEE

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND, INC·Product code IYO·June 27, 2014

    TRANSDUCER S8-3T MICRO TEE

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND, INC.·Product code IYO·January 24, 2014

    HDI 5000 ULTRASOUND STANDARD SYSTEM

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND, INC.·Product code IYO·March 30, 2012

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 2, 2013

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 4, 2011

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 17, 2008

    UNIVERSAL GLENOID - INLAY LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 30, 2019

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSE MANUFACTURING·Product code FKX·August 19, 2011

    TWINFIX ULTRA 5.5MM PLLA/HA 2 UBWHT/BL--Absorbable Suture anchor Product Number: 72202602

    FDA Enforcement
    Class II ·Ongoing·Smith & Nephew, Inc.·October 28, 2020