BEUDAMED
    34 results · 111ms · Sources: EU EUDAMED, US FDA

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    Quality Packaging Specialists International, LLC

    FDA registration
    Quality Packaging Specialists International, LLC·15 products·🇺🇸 United States

    SYRINGE 10ML E/T WITH US GRAPHICS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMF·June 16, 2020

    TERUMO SURGUARD3 SAFETY HYPODERMIC NEEDLE (SHORT SHEATH)

    FDA Adverse Event
    Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·October 15, 2021

    VIDAS® CK MB

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JHX·January 29, 2019

    METASUL HEAD HIP IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·March 20, 2017

    INSERT HIP IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·March 20, 2017

    VIDAS® B·R·A·H·M·S PCT¿

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX SA·Product code PRI·September 30, 2024

    RETRACTABLE SAFETY SCALPEL

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code GDZ·December 11, 2015

    UNKNOWN MÜLLER ROOF REINFORCEMENT RING

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code MEH·June 2, 2017

    JADA SYSTEM

    FDA Adverse Event
    Malfunction ·ORGANON LLC·Product code OQY·September 9, 2025

    PROMETRA II PROGRAMMABLE PUMP

    FDA Adverse Event
    Injury ·FLOWONIX MEDICAL, INC.·Product code LKK·January 19, 2021

    MINI VIDAS® BLUE 110 / 220 V

    FDA Adverse Event
    Malfunction ·BIOMERIEUX ITALIA S.P.A.·Product code JJE·June 26, 2023

    JADA SYSTEM

    FDA Adverse Event
    Malfunction ·ORGANON & CO.·Product code OQY·February 29, 2024

    UNKNOWN DYNESYS SPINE IMPL

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code NQP·September 11, 2017

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·March 24, 2011

    FLEXIBLE SHAFT, TRI-SHANK

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code GFG·October 12, 2017

    SCREW FOR 75.11.00-05

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HTW·March 12, 2018

    SULOX, HEAD, M, 32/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·September 25, 2017

    REVOLVE (OEM VERSION OF GID 700)

    FDA Adverse Event
    Injury ·THE GID GROUP INC.·Product code MUU·April 18, 2014

    GENERAL LAP PACK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code KDD·February 26, 2016