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

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    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·therascreen PIK3CA RGQ PCR Kit

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481124563·LOCATOR R-Tx Attachment System, FairTwo S, Fair...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031257·OsteoFlap Removal Kit

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707069386·BIRD BEAK PLIERS ANGLE STYLE

    BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET PRE-ATTACHED HOLDER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 5, 2024

    SILVERGLIDE

    FDA UDI
    STRYKER CORPORATION·04546540532213·Non-Stick Bipolar Electrosurgical Precision For...

    SilverGlide

    FDA UDI
    STRYKER CORPORATION·04546540695840·ProSeries Non-stick Bipolar Electrosurgical For...

    SILVERGLIDE

    FDA UDI
    STRYKER CORPORATION·04546540714848·Non-Stick Bipolar Electrosurgical Standard Forc...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197499750·Quervain Blade 70x70m...

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·December 10, 2018

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·December 10, 2018

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·December 10, 2018

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 31, 2018

    Analyzer, Medical Image

    FDA Pre-Market Approval
    FDA Class 2 ·PARASCRIPT ACCUDETECT 6.1.0

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·PRESILLION PLUS COCR CORONARY STENT RX SYSTEM

    PROCLAIM¿ DRG IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 5, 2019

    GORE TIGRIS® VASCULAR STENT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·October 11, 2016

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·NIRxcell CoCr Coronary Stent on RX System

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·NIRxcell CoCr Coronary Stent on RX System

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·NIRxcell CoCr Coronary Stent on RX System