BEUDAMED
    21 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    METHAQUALONE ENZYME IMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    AXSOS

    FDA UDI
    Stryker GmbH·07613327093582·Tibia Targeting Insert For Tibia Targeting Tray

    Mckesson

    FDA UDI
    MCKESSON MEDICAL-SURGICAL INC.·10612479250724·Extension Feeding Set SINGLE ENFit® PORT Straig...

    Mckesson

    FDA UDI
    MCKESSON MEDICAL-SURGICAL INC.·10612479250755·Extension Feeding Set SINGLE ENFit® PORT Straig...

    ADVIA® Chemistry Reagent Wedge 40 mL

    FDA UDI
    Siemens Healthcare Diagnostics Inc.·00630414601182·ADVIA® Chemistry Reagent Wedge 40 mL

    AUTO SUTURE SURGIPORT SPIRAL SLEEVE

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

    POLARIS SPINAL SYSTEM -TRANSLATION SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    5.5 TI CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    V.A.C. THERAPY

    FDA Adverse Event
    Injury ·KCI USA INC.·Product code OMP·June 19, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·December 22, 2010

    POLARIS SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020

    PEDICLE SCREW UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    PEDICLE SCREW UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    PEDICLE SCREW UNKNOWN TYPE/SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    CANNULATED TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·December 3, 2020

    BD UNSPECIFIED IV PIGGYBACK SECONDARY SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·October 13, 2023

    4.0MM TI LOCKING SCREW W/T25 STARDRIVE 54MM F/IM NAILS-STER

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code HSB·January 27, 2017

    POLARIS TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019