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 61326-2-6:2013

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment

Oct 31, 2013
95.99   Withdrawal of Standard   Dec 30, 2024

General information

95.99     Dec 30, 2024

ISS

N065

European Norm

17.220     25.040.40     33.100  

English  

Van plana za 2013.

Buying

Withdrawn

Language in which you want to receive the document.

Scope

IEC 61326-2-6:2012 specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment. This second edition cancels and replaces the first edition published in 2005 and constitutes a technical revision. It includes the following significant technical change: update of the document with respect to IEC 61326-1:2012.

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

Life cycle

NOW

WITHDRAWN
SRPS EN 61326-2-6:2013
95.99 Withdrawal of Standard
Dec 30, 2024

REVISED BY

PUBLISHED
SRPS EN IEC 61326-2-6:2021

Related project

Adopted from EN 61326-2-6:2013