BEUDAMED
    19 results · 21ms · Sources: EU EUDAMED, US FDA

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    COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016692·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016739·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016715·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·00848486016708·Tibial Bearing Insert

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386356·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 8 - 8 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386271·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 8 - 9 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386325·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 8 - 10 MM

    Mako

    FDA UDI
    MAKO SURGICAL CORP.·07613327386301·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 8 - 12 MM

    THERMO SCIENTIFIC MAS OMNI-CORE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DENTRON SENSOR

    FDA 510(k)
    FDA Class 2 ·Dental

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·October 17, 2014

    FENESTRATED BIPOLAR FORCEPSINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 20, 2013

    HEARTMATE II SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·May 5, 2011

    UNID ROD

    FDA Adverse Event
    Malfunction ·MEDICREA INTERNATIONAL SA·Product code MNI·July 29, 2024

    UNID ROD

    FDA Adverse Event
    Malfunction ·MEDICREA INTERNATIONAL SA·Product code MNI·July 29, 2024

    CARTO 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·December 14, 2023

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 9, 2026

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 10, 2026