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CEN

FprEN ISO 18113-3

(Main)

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/FDIS 18113-3:2022)

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/FDIS 18113-3:2022)

This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for professional use.
This document also applies to apparatus and equipment intended to be used with IVD instruments for professional use.
This document can also be applicable to accessories.
This document does not apply to:
a) instructions for instrument servicing or repair;
b) IVD reagents, including calibrators and control materials for use in control of the reagent;
c) IVD instruments for self-testing.

In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller - Teil 3: Geräte für in-vitro-diagnostische Untersuchungen zum Gebrauch durch Fachpersonal (ISO/FDIS 18113-3:2022)

Dieses Dokument legt Anforderungen an die durch den Hersteller von in-vitro-diagnostischen (IVD )Geräten für den Gebrauch durch Fachpersonal bereitgestellten Informationen fest.
Dieses Dokument gilt auch für Geräte und Ausrüstungen, die für den Gebrauch zusammen mit IVD Geräten für den Gebrauch durch Fachpersonal vorgesehen sind.
Dieses Dokument kann auch auf Zubehör angewendet werden.
Dieses Dokument gilt nicht für:
a)   Anweisungen für die Geräteinstandhaltung oder  reparatur;
b)   IVD Reagenzien, einschließlich Kalibriermaterialien und Kontrollmaterialien zur Kontrolle des Reagenz;
c)   IVD Geräte zur Eigenanwendung.

Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 3: Instruments de diagnostic in vitro à usage professionnel (ISO/FDIS 18113-3:2022)

Le présent document spécifie les exigences relatives aux informations fournies par le fabricant d’instruments de diagnostic in vitro (DIV) à usage professionnel.
Le présent document s’applique aussi aux appareillages et équipements destinés à être utilisés avec les instruments de DIV à usage professionnel.
Le présent document peut aussi s’appliquer aux accessoires.
Le présent document ne s’applique pas à ce qui suit :
a) instructions d’entretien ou de réparation des instruments ;
b) réactifs de DIV, y compris les étalons et les matériaux de contrôle à utiliser dans le contrôle du réactif ;
c) instruments de DIV destinés à des autodiagnostics.

In vitro diagnostični preskusni sistemi - Informacije proizvajalca (označevanje) - 3. del: Diagnostični instrumenti in vitro za poklicno uporabo (ISO/FDIS 18113-3:2022)

General Information

Status
Not Published
Publication Date
01-Dec-2022
ICS
11.100.10 - In vitro diagnostic test systems
Technical Committee
CEN/TC 140 - In vitro diagnostic systems
Drafting Committee
CEN/TC 140 - In vitro diagnostic systems
Current Stage
6055 - CEN Ratification completed (DOR) - Publishing
Start Date
02-Oct-2022
Completion Date
02-Oct-2022
Directive
2017/746 - Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU
Mandate
M/481 - Mandate to CEN, CENELEC and ETSI for Standardisation in the fieid of household dishwasher
M/575 - Medical devices in support of Regulation (EU) 2017/745 and in vitro diagnostic medical devices in support of Regulation (EU) 2017/746
Ref Project
kSIST FprEN ISO 18113-3:2022 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/FDIS 18113-3:2022)

Relations

Revises
EN ISO 18113-3:2011 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
Effective Date
27-Nov-2019

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SLOVENSKI STANDARD
oSIST prEN ISO 18113-3:2021
01-oktober-2021
In vitro diagnostični preskusni sistemi - Informacije proizvajalca (označevanje) - 3.
del: Diagnostični instrumenti in vitro za poklicno uporabo (ISO/DIS 18113-3:2021)
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling)
- Part 3: In vitro diagnostic instruments for professional use (ISO/DIS 18113-3:2021)
In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller - Teil 3:
Geräte für in-vitro-diagnostische Untersuchungen zum Gebrauch durch Fachpersonal
(ISO/DIS 18113-3:2021)
Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant
(étiquetage) - Partie 3: Instruments de diagnostic in vitro à usage professionnel (ISO/DIS
18113-3:2021)
Ta slovenski standard je istoveten z: prEN ISO 18113-3
ICS:
11.100.10 Diagnostični preskusni In vitro diagnostic test
sistemi in vitro systems
oSIST prEN ISO 18113-3:2021 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------
oSIST prEN ISO 18113-3:2021

---------------------- Page: 2 ----------------------
oSIST prEN ISO 18113-3:2021
DRAFT INTERNATIONAL STANDARD
ISO/DIS 18113-3
ISO/TC 212 Secretariat: ANSI
Voting begins on: Voting terminates on:
2021-08-02 2021-10-25
In vitro diagnostic medical devices — Information supplied
by the manufacturer (labelling) —
Part 3:
In vitro diagnostic instruments for professional use
Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) —
Partie 3: Instruments de diagnostic in vitro à usage professionnel
ICS: 11.100.10
THIS DOCUMENT IS A DRAFT CIRCULATED
This document is circulated as received from the committee secretariat.
FOR COMMENT AND APPROVAL. IT IS
THEREFORE SUBJECT TO CHANGE AND MAY
NOT BE REFERRED TO AS AN INTERNATIONAL
STANDARD UNTIL PUBLISHED AS SUCH.
IN ADDITION TO THEIR EVALUATION AS
ISO/CEN PARALLEL PROCESSING
BEING ACCEPTABLE FOR INDUSTRIAL,
TECHNOLOGICAL, COMMERCIAL AND
USER PURPOSES, DRAFT INTERNATIONAL
STANDARDS MAY ON OCCASION HAVE TO
BE CONSIDERED IN THE LIGHT OF THEIR
POTENTIAL TO BECOME STANDARDS TO
WHICH REFERENCE MAY BE MADE IN
Reference number
NATIONAL REGULATIONS.
ISO/DIS 18113-3:2021(E)
RECIPIENTS OF THIS DRAFT ARE INVITED
TO SUBMIT, WITH THEIR COMMENTS,
NOTIFICATION OF ANY RELEVANT PATENT
RIGHTS OF WHICH THEY ARE AWARE AND TO
©
PROVIDE SUPPORTING DOCUMENTATION. ISO 2021

---------------------- Page: 3 ----------------------
oSIST prEN ISO 18113-3:2021
ISO/DIS 18113-3:2021(E)

COPYRIGHT PROTECTED DOCUMENT
© ISO 2021
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2021 – All rights reserved

---------------------- Page: 4 ----------------------
oSIST prEN ISO 18113-3:2021
ISO/DIS 18113-3:2021(E)

Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Essential requirements . 2
5 Labels and marking .
...

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