BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    VOLU-SOL EOSIN Y STAIN

    FDA 510(k)
    FDA Class 1 ·Hematology

    STAT DL 9.5 FR. 34 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·August 11, 1998

    U-RIGHT EAR THEMOMETER, MODELS TD-1115 AND TD-1118

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CADD CHECKVALVE ADMINISTRATION SET, MODEL 21-7090

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CONSERVE(R) PLUS CUP

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code KWA·May 8, 2014

    PIP SZ. 30 PROXIMAL

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS·Product code MPK·October 18, 2012

    COMPRESSION ANASTOMOSIS RING CAR 27/COLONRING

    FDA Adverse Event
    Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 10, 2010

    Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021