BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    VALLEYLAB LAPAROSCOPIC HANDSWITCH/ELECTRODES

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

    Stern Snap One Piece Abutment 1mm Cuff (B)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549111921·The SternSnap Attachment is indicated for use w...

    NO-PROFILE

    FDA UDI
    Biomet Sports Medicine, LLC·00880304406032·

    Valencia Pedicle Screw System

    FDA UDI
    Altus Spine, LLC·B41799045601·4.5mm x 60mm Dual Lead Closed Head Screw

    ROCHE COBAS READY ALKALINE PHOSPHATASE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 4/12 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 23, 2021

    MODULAR FINNED STEM 40MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 16, 2019

    VANGUARD FEMORAL RT 70

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 16, 2019

    RENEGADE HI-FLO MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KRA·November 22, 2010

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 30, 2012

    REGENEREX PATELLA 34MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 16, 2019