BEUDAMED
    26 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Visco (olifilcon A) soft contact lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Expiratory valve set

    FDA UDI
    Hamilton Medical AG·07630002801133·Expiratory valve set for HAMILTON-C2/C3/C6, adu...

    NA

    FDA UDI
    MAKO SURGICAL CORP.·00848486003142·FEMORAL ARRAY EXTENDED POST

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017835·K-Wire, Double Ended, Trocar Point, Diameter Si...

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5821602450·SCISSORS, SURGICAL TISSUE, DENTAL

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613084875·K-Wire, Double Ended, Trocar Point, Diameter 0....

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613084882·K-Wire, Double Ended, Trocar Point, Diameter 0....

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197416757·Myers Vein Stripper 9mm di...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197416764·Myers Vein Stripper 16mm d...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197416771·Myers Vein Stripper 12.5mm...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197416740·Myers Vein Stripper 6mm di...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613084899·K-Wire, Double Ended, Trocar Point, Diameter 0....

    Distal Cut Adaptor

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215031633·

    HS/HG PROSTHETIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    HARMONIC SCALPEL BLADES AND SHEARS

    FDA 510(k)
    FDA Unclassified ·Unknown

    SET, ADMINISTRATION, INTRAVASCULAR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016

    FEMORAL ARRAY POST ASSEMBLY

    FDA Adverse Event
    Injury ·MAKO SURGICAL CORP.·Product code OLO·March 11, 2016

    GORE DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DYB·October 19, 2020

    GORE® DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DYB·October 6, 2016

    STOPCOCK MANIFOLD GANGS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FMG·June 17, 2020