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

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    MODIFICATION TO VERSABOND BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Baltic Denture System BDLoad

    FDA UDI
    Merz Dental GmbH·D7091033509·Baltic Denture System BDLoad BDLoad ↓ Mm6 PLSEu...

    DBB-05 HEMODIALYSIS DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    FLEXICAST

    FDA 510(k)
    FDA Class 2 ·Dental

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DTK·August 21, 2014

    UNK

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DTK·August 20, 2014

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·August 20, 2014

    LOCKING HOLDING SLEEVE-LONG FOR MATRIX

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code LXH·April 3, 2013

    SWIFT-LOCK ANCHOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIV.·Product code LGW·March 24, 2011

    HOMECHOICE CYCLER-REFURBISHED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·April 23, 2008

    GUNTHER TULIP VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·April 3, 2026

    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

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·December 5, 2017

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·November 1, 2017

    GUNTHER TULIP VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·November 4, 2025

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 27, 2018

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·May 5, 2017

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·May 12, 2017

    UNKNOWN

    FDA Adverse Event
    Injury ·Product code DTK·August 20, 2020

    UNK

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DTK·August 20, 2014