IEC 61010-2-101:2002 ED1

Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment

Publication date: Jan 9, 2002

General information

Current stage: 99.60 Effective date: Jan 22, 2015

Originator: IEC

Owner: TC 66

Type: International Standard

ICS: 11.040.55 19.08

Languages: English French Spanish

Buying

Status: Revised

PDF - ALL 16,395

Paper - ALL 16,395

CD - ALL 16,395

Language

Language in which you want to receive the document.

Scope

Applies to equipment intended for in vitro diagnostic (IVD) medical purposes. This is used for the examination of specimens, including blood and tissue samples, derived from the human body. The standard also covers self-test IVD medical equipment for use by lay persons.

Life cycle

NOW

IEC 61010-2-101:2002 ED1
99.60 Withdrawal effective
Jan 22, 2015

REVISED BY

IEC 61010-2-101:2015 ED2

Preview

Only informative sections of projects are publicly available. To view the full content, you will need to members of the committee. If you are a member, please log in to your account by clicking on the "Log in" button.