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DIN EN 12470-3:2009-11

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

CLINICAL THERMOMETERS - PART 3: PERFORMANCE OF COMPACT ELECTRICAL THERMOMETERS (NON-PREDICTIVE AND PREDICTIVE) WITH MAXIMUM DEVICE
Available format(s)

Hardcopy , PDF

Superseded date

01-02-2013

Language(s)

English

Published date

01-01-2009

Vorwort
1 Anwendungsbereich
2 Normative Verweisungen
3 Begriffe
4 Einheit
5 Thermometerarten
6 Anforderungen
7 Prüfverfahren
8 Bereitstellung von Informationen durch den Hersteller
Anhang A (informativ) Vorgeschlagene Arten von
          Prüfungen nach den Anforderungen dieser
          Norm
Anhang B (informativ) Literaturhinweise
Anhang ZA (informative) Zusammenhang zwischen dieser
          Europäischen Norm und den grundlegenden
          Anforderungen der EG-Richtlinie 93/42 EWG

Describes the performance requirements for compact clinical electrical thermometers with maximum device (non-predictive and predictive).

DocumentType
Standard
Pages
24
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Superseded
SupersededBy

BWB TL 6515-0007 : 1ED 2008 DIGITAL FEVER THERMOMETER

IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
ISO 2859-2:1985 Sampling procedures for inspection by attributes — Part 2: Sampling plans indexed by limiting quality (LQ) for isolated lot inspection
EN 60601-1-2:2015 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
EN 1041:2008+A1:2013 Information supplied by the manufacturer of medical devices
ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
EN 980:2008 Symbols for use in the labelling of medical devices
EN ISO 10993-1:2009/AC:2010 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010)

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$143.06
Including GST where applicable

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