• There are no items in your cart

I.S. EN 592:2002

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

INSTRUCTIONS FOR USE FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR SELF-TESTING

Available format(s)

Hardcopy , PDF

Superseded date

29-12-2009

Superseded by

I.S. EN ISO 18113-5:2009

Language(s)

English

Published date

01-01-2002

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.


Dates of withdrawal of national standards are available from NSAI.

€33.00
Excluding VAT

Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Form and presentation of the instructions for use
5 Requirements for the content of the instructions for
  use
6 Requirements for supplementary information
Annex ZA (informative) Clauses of this European Standard
         addressing essential requirements or other
         provisions of EU Directives
Bibliography

Specifies the requirements for the contents of instructions for use in for vitro diagnostic instruments including apparatus and equipment for self-testing.

DocumentType
Standard
Pages
12
PublisherName
National Standards Authority of Ireland
Status
Superseded
SupersededBy

Standards Relationship
UNE-EN 592:2002 Identical
NS EN 592 : 2002 Identical
NF EN 592 : 2002 Identical
EN 592 : 2002 Identical
NEN EN 592 : 2002 Identical
BS EN 592:2002 Identical
SN EN 592 : 2002 Identical
UNI EN 592 : 2002 Identical
DIN EN 592:2002-05 Identical
NBN EN 592 : 2002 Identical
DIN EN 592:1994-11 Identical

EN 591 : 2001 INSTRUCTIONS FOR USE FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR PROFESSIONAL USE
EN 376 : 2002 INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING
ISO 8601:2004 Data elements and interchange formats Information interchange Representation of dates and times
EN 375 : 2001 INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE
ISO/IEC Guide 2:2004 Standardization and related activities — General vocabulary
EN 61010-1:2010 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements
EN 28601 : 1992 DATA ELEMENTS AND INTERCHANGE FORMATS - INFORMATION INTERCHANGE - REPRESENTATION OF DATES AND TIMES
IEC 61010-1:2010+AMD1:2016 CSV Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements
EN 980:2008 Symbols for use in the labelling of medical devices

Access your standards online with a subscription

Features

  • Simple online access to standards, technical information and regulations.

  • Critical updates of standards and customisable alerts and notifications.

  • Multi-user online standards collection: secure, flexible and cost effective.