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

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    Filters Regulation: Us FDA ×

    RANDOX IGE

    FDA 510(k)
    FDA Class 2 ·Immunology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526743625·LEVAMED ANKLE SUPPORT SAND V

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517275097·CoRoent® XL+, 10x18x55mm

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR50108551·Arch wire tucker

    GUNTHER TULIP VENA CAVA MREYE FILTER SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COOK VASCULAR ELECTROSURGICAL DISSECTION SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·June 13, 2016

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

    *

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·June 17, 2016

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·June 9, 2016

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·June 2, 2016

    GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·June 2, 2016

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·June 13, 2016

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·June 13, 2016

    UNKNOWN

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·June 13, 2016