EN 60601-2-9:1996/corrigendum:1996
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.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
01-05-2007
12-01-2013
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
Defines particular requirements for safety of dosemeters for use in medical practice in the patient environment for radiotherapy.
| Committee |
TC 62
|
| DevelopmentNote |
To be read in conjunction with EN 60601-1, EN 60601-1-1 and EN 60601-1-2. Supersedes HD 395.2.9 (05/2001)
|
| DocumentType |
Standard
|
| PublisherName |
European Committee for Standards - Electrical
|
| Status |
Withdrawn
|
| Supersedes |
| Standards | Relationship |
| NF EN 60601 2-9 : 1997 | Identical |
| IEC 60601-2-9:1996 | Identical |
| NBN EN 60601 2-9 : 1997 | Identical |
| I.S. EN 60601-2-9:1998 | Identical |
| PN EN 60601-2-9 : 2006 | Identical |
| SN EN 60601-2-9 : 1996 | Identical |
| DIN EN 60601-2-9 : 1999 | Identical |
| VDE 0750-2-9 : 1999 | Identical |
| UNE-EN 60601-2-9:1997 | Identical |
| BS EN 60601-2-9:1997 | Identical |
| CEI EN 60601-2-9 : 1998 | Identical |
| 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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