• UNI/TR 11408 : 2011

    Current The latest, up-to-date edition.

    GUIDE TO DESIGN, DEVELOPMENT AND CONTROL OF A RECONDITION PROCESS FOR REUSABLE MEDICAL DEVICES THAT SHALL BE STERILIZED BY STEAM

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    Published date:  03-03-2011

    Publisher:  Ente Nazionale Italiano di Unificazione (UNI)

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    Table of Contents - (Show below) - (Hide below)

    1 SCOPO E CAMPO DI APPLICAZIONE
    2 RIFERIMENTI NORMATIVI
    3 TERMINI E DEFINIZIONI
    4 PROCESSO DI RICONDIZIONAMENTO DI DM RIUTILIZZABILI
       STERILIZZABILI A VAPORE
    5 DECONTAMINAZIONE
    6 LAVAGGIO
    7 DISINFEZIONE
    8 ASCIUGATURA
    9 MONTAGGIO E CONTROLLO DEL DM
    10 RICOMPOSIZIONE DEL KIT
    11 CONFEZIONAMENTO
    14 RILASCIO DEL DM RICONDIZIONATO
    15 MOVIMENTAZIONE E STOCCAGGIO DEI DM STERILI
    16 PERSONALE
    17 RESPONSABILITA CHIAVE
    18 FORMAZIONE E COMPETENZE
    19 AMBIENTI
    20 MANUTENZIONE DELLE APPARECCHIATURE E DEI DM
    21 CONTROLLI E VERIFICHE PERIODICHE
    22 CONVALIDE
    23 DOCUMENTAZIONE
    25 RIESAME DEL PROCESSO
    26 TRACCIABILITA
    APPENDICE A (informativa) - CRITERI DI CONFIGURAZIONE E
       DIMENSIONAMENTO STRUTTURALE E TECNOLOGICO DI UN IMPIANTO
       DI RICONDIZIONAMENTO
    APPENDICE B (informativa) - NORME COMPORTAMENTALI

    General Product Information - (Show below) - (Hide below)

    Committee CT 44
    Document Type Technical Report
    Publisher Ente Nazionale Italiano di Unificazione (UNI)
    Status Current

    Standards Referencing This Book - (Show below) - (Hide below)

    UNI EN ISO 14644-3 : 2006 CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 3: TEST METHODS
    UNI EN 556-1 : 2002 Sterilization of medical devices - Requirements for medical devices to be designated “STERILE” - Requirements for terminally sterilized medical devices
    UNI EN ISO 11607-2 : 2014 PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES
    UNI EN 13060 : 2010 SMALL STEAM STERILIZERS
    UNI EN ISO 14644-1 : 2001 CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - CLASSIFICATION OF AIR CLEANLINESS
    UNI EN ISO 14644-2 : 2001 CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 2: MONITORING TO PROVIDE EVIDENCE OF CLEANROOM PERFORMANCE RELATED TO AIR CLEANLINESS BY PARTICLE CONCENTRATION
    UNI EN ISO 17665-1 : 2007 STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES
    UNI EN ISO 13485 : 2004 MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - REQUIREMENTS FOR REGULATORY PURPOSES
    UNI CEN ISO/TS 17665-2 : 2009 STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ISO 17665-1
    UNI EN ISO 15882 : 2009 STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - GUIDANCE FOR SELECTION, USE AND INTERPRETATION OF RESULTS
    UNI EN 285 : 2009 STERILIZATION - STEAM STERILIZERS - LARGE STERILIZERS
    UNI EN ISO 11140-1 : 2009 STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - PART 1: GENERAL REQUIREMENTS
    UNI EN 14971 : 2006 TEXTILES - KNITTED FABRICS - DETERMINATION OF NUMBER OF STITCHES PER UNIT LENGTH AND UNIT AREA
    UNI EN ISO 11607-1 : 2014 PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS
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