BEUDAMED
    20 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Mini Ridge Filter and auxiliary functions for PROBEAT-V

    FDA 510(k)
    FDA Class 2 ·Radiology

    CLEARARCH

    FDA 510(k)
    FDA Class 2 ·Dental

    SONOACE X6 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ULTRATHANE DAWSON-MUELLER MAC-LOC LOCKING LOOP MULTIPURPOSE DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GBO·April 11, 2019

    KRD DEVICE, EMBOLIZATION, VASCULAR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 19, 2019

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 27, 2011

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 21, 2013

    ZERO TIP NITINOL STONE RETRIEVAL BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FFL·September 30, 2008

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·June 20, 2019

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 17, 2018

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·September 17, 2018

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·January 2, 2020

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·January 2, 2020

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·March 11, 2020

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·July 31, 2019

    SECURESTRAP UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GDW·August 27, 2018

    MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAN·August 27, 2018

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·February 25, 2019

    PHYSIOMESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 27, 2018

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·February 3, 2020