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I.S. EN 60601-2-9:1998

Withdrawn
Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF PATIENT CONTACT DOSEMETERS USED IN RADIOTHERAPY WITH ELECTRICALLY CONNECTED RADIATION DETECTORS
Available format(s)

Hardcopy , PDF

Withdrawn date

09-06-2016

Language(s)

English

Published date

06-02-1998

Preview

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.

FOREWORD
INTRODUCTION
SECTION ONE - GENERAL
  1 Scope and object
  2 Terminology and definitions
  5 Classification
  6 Identification, marking and documents
SECTION TWO - ENVIRONMENTAL CONDITIONS
SECTION THREE - PROTECTION AGAINST ELECTRIC SHOCK HAZARDS
  15 Limitation of voltage and/or energy
SECTION FOUR - PROTECTION AGAINST MECHANICAL HAZARDS
  21 Mechanical Strength
SECTION FIVE - PROTECTION AGAINST HAZARDS FROM UNWANTED OR
               EXCESSIVE RADIATION
SECTION SIX - PROTECTION AGAINST HAZARDS OF IGNITION OF FLAMMABLE
              ANAESTHETIC MIXTURES
SECTION SEVEN - PROTECTION AGAINST EXCESSIVE TEMPERATURES AND
                OTHER SAFETY HAZARDS
  44 Overflow, spillage, leakage, humidity, ingress of liquids,
     sterilization and disinfection
SECTION EIGHT - ACCURACY OF OPERATING DATA AND PROTECTION
                AGAINST HAZARDOUS OUTPUT
  50 Accuracy of operating data
SECTION NINE - ABNORMAL OPERATION AND FAULT CONDITIONS;
ENVIRONMENTAL TESTS
SECTION TEN - CONSTRUCTIONAL REQUIREMENTS
Appendix L - References - Publications mentioned in this Standard
Annex AA - Index of defined terms
Annex ZA (normative) Normative references to international
         publications with their corresponding European
         publications
Annex ZB (informative) Normative references to international
         publications with their corresponding European
         publications

Specifies particular requirements for the safety of dosimeters used in medical practice in the patient environment for radiotherapy.

DevelopmentNote
Supersedes I.S. HD 395-2-9. (10/2011)
DocumentType
Standard
Pages
42
PublisherName
National Standards Authority of Ireland
Status
Withdrawn
Supersedes

IEC 60731:2011+AMD1:2016 CSV Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy
IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
IEC TR 60788:2004 Medical electrical equipment - Glossary of defined terms
EN 60601-1-1:2001 Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems
HD 534 : 200S1 MEDICAL ELECTRICAL EQUIPMENT. DOSIMETERS WITH IONIZATION CHAMBERS AS USED IN RADIOTHERAPY
IEC 60601-1-2:2014 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
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
HD 501 : 200S1 MEDICAL RADIOLOGY - TERMINOLOGY
EN 61010-1:2010 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements
IEC 61010-1:2010+AMD1:2016 CSV Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements
IEC 60601-1-1:2000 Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems

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