BEUDAMED
    173 results · 96ms · Sources: EU EUDAMED, US FDA

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    PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC

    Manufacturer
    🇺🇸 United States·3 Basic UDI-DIs·9 Devices

    C2 Cryoablation(TM) System catheter

    Device
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 Cryoablation(TM) System catheter

    Device
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 Cryoablation(TM) System catheter

    Device
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 Cryoablation(TM) System catheter

    Device
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 Cryoablation(TM) System catheter

    Device
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 Cryoablation(TM) System catheter

    Device
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 CryoBalloon™ Ablation System Nitroclip

    Device
    EU MDR · Eu Md Class 1 ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 CryoBalloon™Ablation system Catheter

    Device
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 CryoBalloon(TM) System Controller

    Device
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries

    C2 Cryoballoon (TM) Ablation System Nitroclip

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·1 device

    C2 Cryoballoon (TM) System Controller

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·1 device

    C2 Cryoballoon (TM) System Catheter

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·7 devices

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 11, 2017

    PENTAX Europe GmbH

    Authorized representative
    🇩🇪 Germany·4 Manufacturers·142 Devices

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·August 11, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 28, 2018

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 28, 2018

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·March 14, 2016

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 21, 2016