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

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    CONSTELLATION CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040043776·Waxing Inst-PK Thomas

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092116401·Zimmer® TSV-compatible 4.5mm Straight MultiXUni...

    Autosoft90™

    FDA UDI
    Unomedical A/S·05705244014428·Single use infusion set for subcutaneous infusi...

    Affiniti

    FDA UDI
    TORNIER, INC.·00846832024704·GLENOID/TRIAL GRASPER

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092131152·Zimmer® TSV-compatible 4.5mm Straight Multi-Uni...

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014602561·Schure Spine Frame Crank Handle

    18-B IR REMOTE RECEIVER

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787020106·

    18-B REFURB. IR REMOTE REC.

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787020113·

    RENEGADE HI-FLO MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STERIS AMSCO MILLENNIUM STEAM STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OMNIPOD DASH INSULIN MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·April 12, 2021

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 12, 2013

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·February 18, 2011

    PD1200 DEFIBRILLATOR/PACEMAKER

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code LDD·February 14, 2008

    BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000277

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code LJS·February 26, 2020

    BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000277

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Company·May 27, 2020

    ZUMA Z2 7F GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC·Product code DQY·June 12, 2020

    PRODIGY LG STAT SHT LT 12.0MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 2, 2016

    PRODIGY LG STAT LNG LT 13.5MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·June 3, 2018