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

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    Disposable Surgical Mask

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    The humeral stems trials are packaged in a kit for Titan Modular Shoulder System under the following labeling: Catalog Number Product Description TRL092002506 Humeral Stem Trial, 6mm TRL092002507 Humeral Stem Trial, 7mm TRL092002508 Humeral Stem Trial, 8mm TRL092002509 Humeral Stem Trial, 9mm TRL092002510 Humeral Stem Trial, 10mm TRL092002511 Humeral Stem Trial, 11mm TRL092002512 Humeral Stem Trial, 12mm TRL092002513 Humeral Stem Trial, 13mm TRL092002514 Humeral Stem Trial, 14mm TRL092002515 Humeral Stem Trial, 15mm TRL092002516 Humeral Stem Trial, 16mm

    FDA Enforcement
    Class II ·Terminated·Integra LifeSciences Corp.·May 2, 2018

    WHITE KNIGHT MASKS, BLUE, PINK, YELLOW, WHITE MASKS (13 MODELS)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    G-MOPS, MODEL 10030

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

    Widex

    FDA UDI
    Widex A/S·05706069773682·Widex EVOKE E-FS (Lime Green S-330 ) Telecoil, ...

    ENTRUST AT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011

    PROLENE POLYPROPYLENE SUTURE

    FDA Adverse Event
    Death ·ETHICON, INC.·Product code GAW·September 30, 2014

    S-ROM M HEAD 36MM +0

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 2, 2013

    Y-90 THERASPHERE (3 GBQ) CANADA COMM

    FDA Adverse Event
    Death ·BIOCOMPATIBLES UK LIMITED·Product code NAW·June 10, 2021

    UNKN TRIGEN INTERTAN INTERTROCH ANTEGR NAIL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDG·April 8, 2022

    UNK - CONSTRUCTS: PLATE/SCREWS

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·October 19, 2020

    UNK - CONSTRUCTS: PLATE/SCREWS

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·October 19, 2020

    EXCOR BLOOD PUMP PU VALVES, 30 ML IN/OUT Ø9 MM

    FDA Adverse Event
    Malfunction ·BERLIN HEART GMBH·Product code DSQ·August 30, 2018