BEUDAMED
    10 results · 40ms · Sources: EU EUDAMED, US FDA

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    24 FR RESECTOSCOPE SHEATH

    FDA Adverse Event
    Malfunction ·R. WOLF, GMBH·Product code FDC·July 18, 1994

    MENISCUS GRASPING FORCEP BY O'CONNOR

    FDA Adverse Event
    Malfunction ·R. WOLF, GMBH·Product code HTD·October 13, 1994

    ARTHROSCOPIC MENISCUS GRASPING FORCEPS

    FDA Adverse Event
    Malfunction ·R. WOLF, GMBH·Product code GEN·July 18, 1994

    KLEPPINGER FORCEPS

    FDA Adverse Event
    Malfunction ·R. WOLF GMBH·Product code HTD·July 18, 1994

    DOUBLE SPOON FORCEP FOR SINUSCOPY

    FDA Adverse Event
    Malfunction ·R. WOLF, GMBH·Product code KAE·July 18, 1994

    GRASPER AND AMPULLA DILATOR

    FDA Adverse Event
    Malfunction ·R. WOLF, GMBH·July 18, 1994

    GRASPER AND AMPULLAAR DILATOR

    FDA Adverse Event
    Malfunction ·R. WOLF, GMBH·Product code KOE·July 18, 1994

    EFFICIA DFM100

    FDA Adverse Event
    Injury ·PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.·Product code MKJ·November 28, 2023

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code MJP·July 26, 2024

    SAVINA 300

    FDA Adverse Event
    Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code CBK·June 23, 2025