Phone: (011) 7541-421, 3409-301, 3409-335, 6547-293, 3409-310
E-mail: Standards sales: prodaja@iss.rs Education: iss-edukacija@iss.rs Information about standards: infocentar@iss.rs
Stevana Brakusa 2, 11030 Beograd
Main menu

SRPS EN 375:2008

Information supplied by the manufacturer with in vitro diagnostic reagents for professional use

Dec 29, 2008
95.99   Withdrawal of Standard   Jun 28, 2011

General information

95.99     Jun 28, 2011

ISS

Z076

European Norm

01.040.11     11.100  

English  

Buying

Withdrawn

Language in which you want to receive the document.

Scope

This standard specifies the requirements for the information supplied by the manufacturer of in vitro diagnostic reagents including reagent products, calibrators, control materials and kits for professional use, which hereafter are called reagents. Note: This standard can also be applied to accessories.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

98/79/EC

In vitro diagnostic medical devices

Harmonized

Life cycle

NOW

WITHDRAWN
SRPS EN 375:2008
95.99 Withdrawal of Standard
Jun 28, 2011

REVISED BY

WITHDRAWN
SRPS EN ISO 18113-2:2011

Related project

Adopted from EN 375:2001