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IEC 61010-2-041:1995

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-041: Particular requirements for autoclaves using steam for the treatment of medical materials, and for laboratory processes
Available format(s)

Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users

Superseded date

04-14-2005

Language(s)

English - French, Spanish, Castilian

Published date

12-19-1995

Foreword
Introduction
Clause
1 Scope and object
2 Normative references
3 Definitions
4 Tests
5 Marking and documentation
6 Protection against electric shock
7 Protection against mechanical hazards
8 Mechanical resistance to shock and impact
9 Equipment temperature limits and protection against
   the spread of fire
10 Resistance to heat
11 Protection against hazards from fluids
12 Protection against radiation, including laser sources,
   and against sonic and ultrasonic pressure
13 Protection against liberated gases, explosion and
   implosion
14 Components
15 Protection by interlocks
16 Measuring circuits
Annexes

Replacement: Applies to AUTOCLAVES, including those with anautomatic loading and unloading system, which incorporate aPRESSURE VESSEL, using steam within the absolute pressure rangefrom 0 to 500 kPa, and intended for the treatment of medicalmaterials and for laboratory processes, for example forsterilization.This standard has the status of a group safety publication.

DevelopmentNote
Also numbered as BS EN 61010-2.041. (12/2005)
DocumentType
Standard
Pages
47
PublisherName
International Electrotechnical Committee
Status
Superseded
SupersededBy

02/124462 DC : DRAFT DEC 2002 BS EN 285 - STERILIZATION - STEAM STERILIZERS - LARGE STERILIZERS
CSA Z15190 : 2005 : R2010 MEDICAL LABORATORIES - REQUIREMENTS FOR SAFETY
PD 6632:1998 Biotechnology. Laboratories for research, development and analysis. Guidance on the selection of equipment needed for biotechnology laboratories according to the degree of hazard
EN 12738:1999 Biotechnology - Laboratories for research, development and analysis - Guidance for containment of animals inoculated with microorganisms in experiments
EN 12128:1998 Biotechnology - Laboratories for research, development and analysis - Containment levels of microbiology laboratories, areas of risk, localities and physical safety requirements
98/123927 DC : DRAFT AUG 1998 PREN 61010-2-045 - SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL ADN LABORATORY USE, PART 2-045: PARTICULAR REQUIREMENTS FOR WASHER-DISINFECTORS USED IN MEDICAL, PHARMACEUTICAL, VETERINARY AND LABORATORY FIELDS
ISO 13683:1997 Sterilization of health care products Requirements for validation and routine control of moist heat sterilization in health care facilities
ISO 15190:2003 Medical laboratories Requirements for safety
BS ISO 15190:2003 Medical laboratories. Requirements for safety
CSA Z15190 : 2005 : R2015 MEDICAL LABORATORIES - REQUIREMENTS FOR SAFETY
CSA Z15190 : 2005 MEDICAL LABORATORIES - REQUIREMENTS FOR SAFETY
BS EN 12738:1999 Biotechnology. Laboratories for research, development and analysis. Guidance for containment of animals inoculated with microorganisms in experiments
BS EN 12740:1999 Biotechnology. Laboratories for research, development and analysis. Guidance for handling, inactivating and testing of waste
BS EN 12128:1998 Biotechnology. Laboratories for research, development and analysis. Containment levels of microbiology laboratories, areas of risk, localities and physical safety requirements
02/121895 DC : DRAFT APR 2002 BS EN 13060 - SMALL STEAM STERILIZERS
CSA ISO 11134 : 0 STERILIZATION OF HEALTH CARE PRODUCTS - REQUIREMENTS FOR VALIDATION AND ROUTINE CONTROL - INDUSTRIAL MOIST HEAT STERILIZATION
04/30048301 DC : DRAFT MAY 2004 BS EN ISO 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES
ISO 11134:1994 Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization

ISO 6718:1991 Bursting discs and bursting disc devices
ISO 3585:1998 Borosilicate glass 3.3 Properties

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