BEUDAMED
    13 results · 27ms · Sources: EU EUDAMED, US FDA

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    IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2

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

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704294279·

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659485617·Steinmann pin 3 Shank End, Diamond Point_x000D_...

    Steinmann pin 3 Shank End, Diamond Point 2.4mm/229mm, Sutur Passer

    FDA UDI
    mahe medical gmbh·EMAHKM718830·Steinmann pin 3 Shank End, Diamond Point 2.4mm/...

    PN 31G 5MM 5B XTW 105BX DE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·April 9, 2021

    BD ANGIOCATH IV CATHETER 24GA 0.75IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·November 21, 2019

    LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM

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

    POWDERED SYNTHETIC (YELLOW) VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PN 31G 5MM 5B XTW 105BX DE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·February 28, 2020

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·April 22, 2013

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code GEI·August 12, 2014

    DEPUY SUMMIT SIZE 9 PROXIMAL POROUS HA COATED STEM

    FDA Adverse Event
    Injury ·DEPUY/JOHNSON AND JOHNSON·Product code KWY·April 21, 2011

    NIBP CUFFS

    FDA Adverse Event
    Injury ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code OED·August 8, 2025