BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    ACSYS SELFTAP ACETABULAR CUP PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902140873·Pediatric Two-Lumen Central Venous Catheterizat...

    SAWYER RECTAL RETRACTOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896020153·SAWYER RECTAL RETRACTOR

    BOHN FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PERCUCATH URINARY CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ARTERIAL LINE NON-MACHINE SPEC 8MM NO D

    FDA Adverse Event
    Malfunction ·ERIKA DE REYNOSA·Product code FJK·February 3, 1999

    ARTERIAL LINE NON-MACHINE SPEC 8MM NO D

    FDA Adverse Event
    Malfunction ·ERIKA DE REYNOSA·Product code FJK·March 1, 1999

    GYNECARE MORCELLEX TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code HET·June 27, 2014

    UNK

    FDA Adverse Event
    Other ·BREG, INC.·Product code ILO·November 8, 2010

    UPHOLD VAGINAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·January 7, 2013

    SMR CEMENTLESS FINNED STEM Ø22

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·December 18, 2018

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021