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

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    NeoSpan Compression Staple Impant w/instruments

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Cavitron®

    FDA UDI
    Dentsply Professional·D00381614261·Cavitron® touch™ Package. Contains: Cavitron To...

    Oticon

    FDA UDI
    Oticon A/S·05707131305473·SENSEI SP, BTE 13 WL 110 PPI

    OXYGEN CONCENTRATOR FILTERS, MODELS DBF32, DBF24, DBF27, DBF25, DFC06 AND DDF47

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CEROS TCP GRANULES

    FDA 510(k)
    FDA Class 2 ·Dental

    SINGLE LUMEN PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LJS·December 19, 2017

    DEPUY1 GENTAMICIN CEMENT 40G

    FDA Adverse Event
    Injury ·9610921 DEPUY CMW·Product code LOD·June 11, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 13, 2011

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 17, 2008

    PATIENT SPECIFIC SMILES TOTAL KNEE REPLACEMENT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·May 13, 2016

    TURBO-FLO SINGLE LUMEN CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·October 1, 2018

    TURBO-FLO SINGLE LUMEN CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·October 1, 2018

    MEDISLIM

    FDA Adverse Event
    Injury ·MEDICREATIONS, LLC·Product code GEX·April 27, 2020