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

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    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·TECHNOMED INTERNATIONAL SONOLITH 2000

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·TECHNOMED INTERNATIONAL SONOLITH 2000

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·TECHNOMED INTERNATIONAL SONOLITH 2000

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·TECHNOMED INTERNATIONAL SONOLITH 3000 (LITHORAY)TM

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·TECHNOMED INTERNATIONAL SONOLITH 2000

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·SONOLITH 3000 LITHOTRIPTER

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·TECHNOMED INTERNATIONAL SONOLITH 2000

    Lithotriptor, Extracorporeal Shock-Wave, Urological

    FDA Pre-Market Approval
    FDA Class 2 ·TECHNOMED INTERNATIONAL SONOLITH 3000

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989052152·LOWER RIGHT SECOND MOLAR TRIMLINE BAND SIZE 11

    Sonova

    FDA UDI
    Sonova AG·07613389310979·myPhonak app

    Epredia

    FDA UDI
    RICHARD-ALLAN SCIENTIFIC COMPANY·00673693089463·"Elastic Stain Kit and its components are used ...

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613098681·Fiberoptic Retractor, Smooth Blades, 5mm Fibero...

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867385368·BB-Tak, Non-Threaded

    BARD-PARKER

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL·Product code GES·July 10, 2020

    DESS dental smart solutions

    FDA UDI
    TERRATS MEDICAL SL.·08435457209607·Internal Hex "Click"

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209132775·

    REVISED LABELING FOR ADX PHENCYCLIDINE

    FDA 510(k)
    FDA Unclassified ·Unknown

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    SILICONE ULTRAVIOLET ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    LinkSymphoKnee

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575247615·Femoral Component, CR