BEUDAMED
    46 results · 37ms · Sources: EU EUDAMED, US FDA

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    Arm Blood Pressure Monitor, Wrist Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526814721·GENUMEDI PSS GREEN O

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526768475·GENUMEDI PSS GREEN III

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304239517·

    Oticon

    FDA UDI
    Oticon A/S·05707131289179·H11V2 TI, MINIRITE 312 WL CNB

    Symmetry Surgical Ultra®

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482049051·Ultra Instruments Clamp; Bulldog Vein Clamp; St...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197541824·RZ Tebbet Breast Retractor 150x30...

    KENEX

    FDA UDI
    KENEX (ELECTRO-MEDICAL) LIMITED·05055449403788·150/430/3130 Mach LED 150F Ceiling System

    URGOTUL AG, ANTIMICROBIAL WOUND DRESSING WITH SILVER

    FDA 510(k)
    FDA Unclassified ·Unknown

    MERITS HEALTH PRODUCTS OXYGEN CONCENTRATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962110942·BULLDOG VEIN CLAMP, 1 1/8", STR, TITANIUM

    Widex

    FDA UDI
    Widex A/S·05706069887532·WIDEX MOMENT M-IM (Light beige ) 330, Right

    Widex

    FDA UDI
    Widex A/S·05706069655568·Widex UNIQUE U-IM (Clay brown ) 330, Right

    Widex

    FDA UDI
    Widex A/S·05706069887549·WIDEX MOMENT M-IM (Clay brown ) 330, Right

    Widex

    FDA UDI
    Widex A/S·05706069887556·WIDEX MOMENT M-IM (Dark brown ) 330, Right

    Widex

    FDA UDI
    Widex A/S·05706069655551·Widex UNIQUE U-IM (Light beige ) 330, Right

    Widex

    FDA UDI
    Widex A/S·05706069655575·Widex UNIQUE U-IM (Dark brown ) 330, Right

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 12, 2025

    MISAGO RX Self Expanding Peripheral Stem

    FDA Enforcement
    Class II ·Terminated·Terumo Medical Corp·December 7, 2016

    OSS TIBIAL AUGMENT BLOCK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·June 9, 2017