BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    Water Based Personal Lubricant with Flavours

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HHM

    FDA UDI
    Oticon A/S·05707131281975·H150V2, MINIBTE 312 WL 85 DBL HHM

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE

    AQUAFLEX 2 (TEFILCON) CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ATLAS SPINE PIVOTING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·January 7, 2016

    CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 6, 2013

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 3, 2008

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS, INC.·Product code HQL·June 21, 2011

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    VITAL-PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·May 24, 2016

    3005180920-2018-00582

    FDA Adverse Event
    Injury ·July 30, 2018