BEUDAMED
    17 results · 19ms · Sources: EU EUDAMED, US FDA

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    MINIFETON 200

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope

    FDA UDI
    THD SPA·08033737710449·The Light-Score LED rectoscope is a disposable ...

    ACUMED

    FDA UDI
    Acumed LLC·10806378039867·1.5mm Narrow Solid Driver Assembly

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197491136·Table Post for fixation at OP table 610mm,...

    SOFTLINE SPRING CLIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MRJ EXTENDED

    FDA 510(k)
    FDA Class 2 ·Radiology

    SUPERION INDIRECT DECOMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NQO·June 20, 2023

    SUPERION INDIRECT DECOMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NQO·June 20, 2023

    2.7MM TI VA LCKNG SCR SLF-TPNG WITH T8 STARDRIVE RECESS 12MM--STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code HRS·June 23, 2016

    PREVALON AIR TURN AND POSITION SYSTEM

    FDA Adverse Event
    Injury ·SAGE PRODUCTS LLC·Product code FMR·October 9, 2014

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 8, 2014

    PORTEX BLUE LINE ULTRA TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL LTD.·Product code BTO·October 12, 2012

    REPLY

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA CRM S.R.L.·Product code NVZ·August 10, 2010

    ultraView SISH DNP Detection Kit, Catalog Number 05907136001, model 800-098 Immunohistochemistry (IHC) for in vitro diagnostic use.

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code PPM·August 2, 2018

    ultraView SISH DNP Detection Kit, Catalog Number 05907136001, model 800-098 Immunohistochemistry (IHC) for in vitro diagnostic use.

    FDA Enforcement
    Class I ·Terminated·Ventana Medical Systems Inc·September 26, 2018

    ultraView SISH DNP Detection Kit, Ventana Part Number 800-098, Roche GMMI 05907136001 in vitro diagnostic

    FDA Enforcement
    Class I ·Terminated·Ventana Medical Systems Inc·March 7, 2018

    ultraView SISH DNP Detection Kit, Ventana Part Number 800-098, Roche GMMI 05907136001 in vitro diagnostic

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code PPM·December 19, 2017