BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    LACTOSORB HAND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICHELANGELO BUNION SYSTEM - MABS, MODEL: MA6000

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MyDay (Stenfilcon A) ASPHERE, MyDay (Stenfilcon A) TORIC, MyDay (Stenfilcon A) MULTIFOCAL, MyDay (Stenfilcon A) MULTIFOCAL TORIC

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·March 6, 2013

    CAPSURE SENSE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    PROTECTA XT CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014