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

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    AMS LARGE PORE POLYPROPHLENE MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772813858·GENUMEDI PRO SILVER SIZE V

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·34026704624103·

    Ascendant

    FDA UDI
    Choice Spine, LP·10885862261120·

    SEAL & PROTECT PROTECTIVE SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    HYDROFIX VASO SHIELD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    311NNM NARROWAND UV PHTOTHERAPY LIGHT LAMP

    FDA Adverse Event
    Injury ·XUZHOU KERNEL MEDICAL INSTRUMENT EQUIPMENT CO LTD.·Product code FTC·December 22, 2022

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 3/26MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 25, 2021

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·July 6, 2017

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·July 6, 2017

    ADAPTA DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·May 21, 2013

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·September 26, 2014

    UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CFR·May 20, 2011

    UNKNOWN

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017

    UNKNOWN

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017

    GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·October 20, 2017

    Depuy P.F.C. E knee system, TC3 tibial insert; polyethylene tibial insert, Sz 4, 12.5 mm; Ref 96-0541.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005