I.S. EN ISO 18113-2:2009

Name: I.S. EN ISO 18113-2:2009 - IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 2: IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE (ISO 18113-2:2009)
Brand: National Standards Authority of Ireland

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IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 2: IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE (ISO 18113-2:2009)

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

12-29-2009

Publisher

National Standards Authority of Ireland

Withdrawn date

10-31-2011

Superseded by

I.S. EN ISO 18113-2:2011

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Excluding Tax where applicable

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.

DocumentType	Standard
Pages	28
PublisherName	National Standards Authority of Ireland
Status	Withdrawn
SupersededBy	I.S. EN ISO 18113-2:2011
Supersedes	I.S. EN 375:2001

Standards	Relationship
EN ISO 18113-2:2009	Equivalent
BS EN ISO 18113-2:2009	Equivalent
ISO 18113-2:2009	Equivalent

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I.S. EN ISO 18113-2:2009

IN VITRO DIAGNOSTIC MEDICAL DEVICES - INFORMATION SUPPLIED BY THE MANUFACTURER (LABELLING) - PART 2: IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE (ISO 18113-2:2009)

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