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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079487·CERAMO TRADITION X bayo. punch flat foot 2.0x14...

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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079333·CERAMO bayonet punch with ejector, 1,0x180mm wo...

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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079395·CERAMO bayonet punch w.eject. fl.foot, 1,0x180m...

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079470·CERAMO bayonet punch w.eject. fl.foot, 2,0x140m...

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079371·CERAMO bayonet punch with ejector, 2,0x140mm wo...

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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079418·CERAMO bayonet punch w.eject. fl.foot, 2,0x180m...

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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079357·CERAMO bayonet punch with ejector, 1,0x140mm wo...

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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079340·CERAMO TRADITION X bayonet punch 1.0x180mm work...

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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079432·CERAMO bayonet punch w.eject. fl.foot, 4,0x180m...

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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079494·CERAMO bayonet punch w.eject. fl.foot, 4,0x140m...

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    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079517·CERAMO bayonet punch w.eject. fl.foot, 5,0x140m...

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079463·CERAMO TRADITION X bayo. punch flat foot 1.0x14...

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749079456·CERAMO bayonet punch w.eject. fl.foot, 1,0x140m...

    ADAPTA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·January 31, 2013

    Pulse Generator, Permanent, Implantable

    FDA classification
    FDA Class 3 ·Pulse Generator, Permanent, Implantable

    Azure S SR MRI, Model Number W3SR01

    FDA Recall
    Open, Classified ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NVZ·June 4, 2020

    Serena CRT-P MRI, Model Numbers: a) W1TR02, b) W1TR05, c) W4TR02, d) W4TR05

    FDA Recall
    Open, Classified ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NVZ·June 4, 2020

    Medtronic implantable pulse generator: Versa, Dual chamber rate responsive pacemaker (DDDR), Model Number VEDR01

    FDA Recall
    Open, Classified ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NVZ·January 17, 2019

    Medtronic implantable pulse generator: SENSIA, Dual chamber pacemaker (DDD): (a) Model Number SED01 (b) Model Number SEDR01 (c) Model Number SEDRL1

    FDA Recall
    Open, Classified ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NVZ·January 17, 2019

    Medtronic CareLink SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Cobalt Crome application, Software Model Number D00U005; 2. Claria Amplia Compia application, Software Model Number D00U009; 3. Evera MRI application, Software Model Number D00U010; 3. Visia AF application, Software Model Number D00U011; 5. Viva Brava Evera application, Software Model Number D00U012;

    FDA Recall
    Open, Classified ·Medtronic, Inc.·Product code NVZ·June 18, 2025