BEUDAMED
    28 results · 23ms · Sources: EU EUDAMED, US FDA

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    SYNTHES SYNAPSE TRANSCONNECTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3.5MM TI CANCELLOUS POLYAXIAL SCREW 22MM

    FDA Adverse Event
    Injury ·SYNTHES PRODUKTIONS GMBH·Product code NKG·February 8, 2018

    LOCKSCR SYNAPSE TAN

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NKG·February 15, 2018

    LOCKSCR SYNAPSE TAN

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NKG·February 15, 2018

    K090539

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·February 26, 2026

    BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OPART, MODEL MRT-600

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADVANCED

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    DREAMSTATION BIPAP AUTOSV

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code MNS·January 16, 2023

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 20, 2022

    BIPAP AUTOSV ADV SYSTEM ONE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 21, 2022

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·March 12, 2026

    BIPAP AUTOSV ADV

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code MNS·October 31, 2022

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·May 2, 2013

    TRIATHLON PS FEM COMPONENT, CEMENTED

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·September 15, 2014

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 26, 2011

    LINER AND SHELL WITH PLASTIC BARRIER 48 MM I.D. 60 MM O.D.

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 3, 2023

    BIPAP AUTOSV ADVANCED SYSTEM

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·January 28, 2022