ISO 80601-2-56:2009

Title
Abstract

ISO 80601-2-56:2009 applies to the basic safety and essential performance of a clinical thermometer in combination with its accessories, referred to as ME equipment. ISO 80601-2-56:2009 specifies the general and technical requirements for electrical clinical thermometers. ISO 80601-2-56:2009 applies to all electrical clinical thermometers that are used for measuring the body temperature of patients. Clinical thermometers can be equipped with interfaces to accommodate secondary indicators, printing equipment, and other auxiliary equipment to create ME systems. ISO 80601-2-56:2009 does not apply to auxiliary equipment. ME equipment that measures a temperature not as a primary purpose, but as a secondary function, is outside the scope of ISO 80601-2-56:2009. Requirements for ME equipment intended to be used for non-invasive human febrile temperature screening of groups of individuals under indoor environmental conditions are given in IEC 80601-2-59:2008 and such ME equipment is not covered by ISO 80601-2-56:2009.

Issue Date

2009-12-08

Category

MED

Included in IECEE System

2011-08-31

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DISCLAIMER: National differences

The National differences and Group differences, National Deviations and Special National conditions (SNC), are based solely on information provided to the Secretariat by the IECEE Member Bodies and/or NCBs and other sources. The IEC/IECEE is not responsible for, nor will it take any position related to, the accuracy or validity of the information provided. To verify the current status of this type of information, we recommend contacting the Member Body (MB) or National Certification Body (NCB) of the relevant country.

Group Differences are applicable for CENELEC member countries: Austria, Belgium, Bulgaria, Croatia, Cyprus, the Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom.

Group/Country

Reference

Last Modified

Differences

TRF Addendum

CanadaCanada

2015-04-16

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Laboratory Name

City

Country

Responsible National Certification Body

Shanghai

China

Pointe Claire

Canada

Toronto

Canada

New Taipei City

Chinese Taipei

Modiin

Israel

Boxborough,

United States of America

Lake Forest,

United States of America

Guangzhou, Guangdong

China

Fontenay-Aux-Roses

France

TRAPPES

France

Oak Creek

United States of America

Carlsbad,

United States of America

Shenzhen, Guangdong

China

Tampere

Finland

Helsinki

Finland

Puchheim

Germany

Shanghai

China

Guangzhou

China

Tel-Aviv

Israel

Shanghai

China

Shenzhen

China

Yokohama,

Japan

Taoyuan City 333

Chinese Taipei

San Diego

United States of America

Jiangsu

China

Guangzhou

China

München

Germany

Northbrook, IL 60062

United States of America

Huangpu District, Guangzhou

China

Taipei City

Chinese Taipei

Offenbach / Main

Germany

Id

Name

City

Country

13336

Toronto, Ontario

Canada

13607

Baltimore,

United States of America

20269

Modiin

Israel

13371

Kista

Sweden

13365

Singapore

Singapore

13424

IL 60005

United States of America

13343

Fontenay-Aux-Roses

France

13641

Paris Cedex 15

France

13361

Lysaker

Norway

13334

BRUSSELS 1070

Belgium

13342

Helsinki

Finland

13597

Tel-Aviv

Israel

13354

Yokohama

Japan

13345

Nürnberg

Germany

13427

Singapore 609937

Singapore

13346

München

Germany

13340

Ballerup

Denmark

13423

Northbrook

United States of America

13344

Offenbach / Main

Germany

Id

Name

City

Country

13356

Gyeongsangnam-do

Korea, Republic of