BEUDAMED
    9,066 results · 18ms · 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

    Rehadapter™ Mk-I INT

    Device
    EU MDR · Eu Md Class 1 ·Rehadapt GmbH·No longer on the market

    Rehadapter™ Mk-I EU

    Device
    EU MDR · Eu Md Class 1 ·Rehadapt GmbH·No longer on the market·1 country

    Rehadapter™ Pro Mk-I INT

    Device
    EU MDR · Eu Md Class 1 ·Rehadapt GmbH·No longer on the market

    Rehadapter™ Pro Mk-I EU

    Device
    EU MDR · Eu Md Class 1 ·Rehadapt GmbH·No longer on the market

    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