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

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    MKI DENTAL PRODUKT GMBH

    FDA registration
    MKI DENTAL PRODUKT GMBH·1 product·🇩🇪 Germany

    TNS MK I STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    Z KAT FLUROTACTIC GUIDANCE SYSTEM MKI

    FDA 510(k)
    FDA Class 2 ·Neurology

    Single Use Electrosurgical Knife

    FDA UDI
    Micro-Tech (Nanjing) Co., Ltd.·06932503555012·Cutting Knife shape I type,Cutting Knife length...

    Single Use Electrosurgical Knife

    FDA UDI
    Micro-Tech (Nanjing) Co., Ltd.·06932503555029·Cutting Knife shape I type,Cutting Knife length...

    Single Use Electrosurgical Knife

    FDA UDI
    Micro-Tech (Nanjing) Co., Ltd.·06932503555036·Cutting Knife shape I type,Cutting Knife length...

    Single Use Electrosurgical Knife

    FDA UDI
    Micro-Tech (Nanjing) Co., Ltd.·06932503555067·Cutting Knife shape I type,Cutting Knife length...

    Single Use Electrosurgical Knife

    FDA UDI
    Micro-Tech (Nanjing) Co., Ltd.·06932503555043·Cutting Knife shape I type,Cutting Knife length...

    Single Use Electrosurgical Knife

    FDA UDI
    Micro-Tech (Nanjing) Co., Ltd.·06932503555050·Cutting Knife shape I type,Cutting Knife length...

    POOL HOIST MKI

    FDA Adverse Event
    Malfunction ·ARJO, LTD.·Product code FSA·October 8, 2002

    APPOSE ULC

    FDA Adverse Event
    Malfunction ·AMERICAN CYANAMID COMP US SURGICAL·Product code GAG·December 10, 2001

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·August 29, 2008

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·May 19, 2020

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 24, 2021

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 19, 2021

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 24, 2021

    NI

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code MKY·May 19, 2021

    DGW GUIDEWIRE

    FDA Adverse Event
    Malfunction ·CORDIS CORP. (MIAMI)·Product code MKI·September 8, 2003

    ULTRA-SELECT NITINOL GUIDEWIRE

    FDA Adverse Event
    Injury ·MICROVENA CORPORATION·Product code MKI·February 16, 1994

    DGW .035 FC STR 150CM TEF LLT

    FDA Adverse Event
    Injury ·CORDIS CORP (MIAMI)·Product code MKI·June 7, 2000