BEUDAMED
    20 results · 34ms · Sources: EU EUDAMED, US FDA

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    Caplugs, Inc.

    Manufacturer
    🇺🇸 United States

    Caplugs, Inc.

    FDA registration
    Caplugs, Inc.·12 products·🇺🇸 United States

    MDSS GmbH

    Authorized representative
    🇩🇪 Germany·388 Manufacturers·16562 Devices

    ACCESSORIES FOR SPACE PUMPS

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code MRZ·July 7, 2016

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·December 2, 2016

    TruFit CB Plug Size Code Red, 7mm; quantity 1; Part #605-001-03; product labeled as sterile; manufactured by OsteoBiologics, Inc., San Antonio, TX.

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code MQV·September 29, 2006

    TruFit CB Plug Size Code Blue, 9mm; quantity 1; Part #605-001-05; product labeled as sterile; manufactured by OsteoBiologics, Inc., San Antonio, TX.

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code MQV·September 29, 2006

    IMPELLA

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·March 25, 2026

    Aplio XG model SSA-790A Aplio XG (SSA-790A) is a premium-class diagnostic ultrasound system incorporating state-of-the-art technologies. It is provided with the highest level of image quality and operability (reflecting the XG (next Generation) in its name), and can be used with ease for research as well as for routine clinical studies.

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code IYO·June 2, 2010

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·December 1, 2023

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·September 25, 2023

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 2, 2026

    DA VINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 7, 2024

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·September 23, 2016

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 1, 2024

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·February 22, 2024

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 2, 2026

    DAVINCI X

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·August 2, 2025

    Revian Inc. Replacement Kit, 120V AC-5V DC, 2A Wall, Type A Plug

    FDA UDI
    Revian, Inc.·00850003374017·Power adapter replacement kit. The Revian 120V ...

    Micro-Tech Informer Plus Silver Monitor, Model 81830. The firm name on the label is Stanley Security Solutions, Inc., Lincoln, NE. Product Usage: The system is a bed exit system designed to indicate, by alarm or signal, when someone attempts to leave the bed. The system consists of a control unit that is mounted on the bed and a pressure sensitive bed sensor pad that is placed across the width of the bed under the mattress or just beneath the sheets and overlays. The control unit is powered by means of a plug-in type power supply and an alarm cord is used to interface the control unit with the nurse call system.

    FDA Recall
    Terminated ·Stanley Security Solutions, Inc.·Product code KMI·December 13, 2011