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

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    CustomizedBone Service

    FDA 510(k)
    FDA Class 2 ·Neurology

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583029986·ET60 MNR T, 2.4G NFM DPB BL DEMO ENCHANT 60

    COMPREHENSIVE REVERSE SHOULDER

    FDA UDI
    Biomet Orthopedics, LLC·00880304477087·

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486000622·MCK Femoral Component

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197081986·TC Barraquer Micro Needle Holder curved...

    QLASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GLOW BY ENDYMED

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

    BD¿ GENERAL USE STERILE HYPODERMIC NEEDLE

    FDA Adverse Event
    Injury ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·October 2, 2015

    ARTICULEZE M HEAD 36MM +5 K980513

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 14, 2016

    UNKNOWN_SIZE 3 PKA INSERT

    FDA Adverse Event
    Injury ·MAKO SURGICAL CORP.·Product code NPJ·January 17, 2022

    GYNECARE PROLIFT PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·June 20, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

    ZIMMER HEX CANNULATED SCREWDRIVER

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HXX·October 15, 2014

    TUBE K2EDTA PLH 13X75 4.0 PLBL LAV BR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code JKA·September 30, 2019

    Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)

    FDA Enforcement
    Class II ·Ongoing·Medtronic Inc.·November 29, 2017