BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    FO51/F151 GOLF MASSAGER

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Radiolucent Headholder Clamp - Doro

    FDA UDI
    Brainlab SE·04056481004583·

    COLLAGEN REAGENT CAT. NO. 5368

    FDA 510(k)
    FDA Class 2 ·Hematology

    BC 1207 ABUTMENT FIXED

    FDA 510(k)
    FDA Class 2 ·Dental

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·January 14, 2013

    SYNCHRON® LX20 PRO CLINICAL ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·December 3, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 4, 2014

    Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015