iTeh StandardsiTeh Standards
EURUSD
Your shopping cart is empty.
SIST

SIST HD 583 S1:1998

(Main)

Medical electrical equipment - Medical electron accelerators - Functional performance characteristics

Medical electrical equipment - Medical electron accelerators - Functional performance characteristics

Superseded by EN 60976:1999

Medizinische elektrische Geräte - Medizinische Elektronenbeschleuniger - Apparative Qualitätsmerkmale

Appareils électromédicaux - Accélérateurs médicaux d'électrons - Caractéristiques fonctionnelles

Medical electrical equipment - Medical electron accelerators - Functional performance characteristics (IEC 60976:1989)

General Information

Status
Withdrawn
Publication Date
30-Sep-1998
Withdrawal Date
31-Jan-2002
ICS
11.040.50 - Radiographic equipment
11.040.60 - Therapy equipment
Technical Committee
IEMO - Electrical equipment in medical practice
Current Stage
9900 - Withdrawal (Adopted Project)
Start Date
01-Feb-2002
Due Date
01-Feb-2002
Completion Date
01-Feb-2002
Ref Project
HD 583 S1:1991 - Medical electrical equipment - Medical electron accelerators - Functional performance characteristics

Relations

Replaced By
SIST EN 60976:2002 - Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
Effective Date
06-May-2014
Replaced By
SIST EN 60976:2002 - Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
Effective Date
28-Jan-2023

Buy Standard

HD 583 S1:1998HD 583 S1:1998
PreviousNext
Standardization document
HD 583 S1:1998
English language
76 pages
sale 10% off
Preview
sale 10% off
Preview
e-Library read for
1 day

Standards Content (Sample)

SLOVENSKI STANDARD
SIST HD 583 S1:1998
01-oktober-1998
Medical electrical equipment - Medical electron accelerators - Functional
performance characteristics (IEC 60976:1989)
Medical electrical equipment - Medical electron accelerators - Functional performance
characteristics
Medizinische elektrische Geräte - Medizinische Elektronenbeschleuniger - Apparative
Qualitätsmerkmale
Appareils électromédicaux - Accélérateurs médicaux d'électrons - Caractéristiques
fonctionnelles
Ta slovenski standard je istoveten z: HD 583 S1:1991
ICS:
11.040.50 Radiografska oprema Radiographic equipment
11.040.60 Terapevtska oprema Therapy equipment
SIST HD 583 S1:1998 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 2 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 3 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 4 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 5 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 6 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 7 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 8 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 9 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 10 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 11 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 12 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 13 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 14 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 15 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 16 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 17 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 18 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 19 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 20 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 21 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 22 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 23 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 24 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 25 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 26 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 27 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 28 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 29 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 30 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 31 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 32 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 33 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 34 ----------------------

SIST HD 583 S1:1998

---------------------- Page: 35 --------------------
...

Questions, Comments and Discussion

Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.

This May Also Interest You

SIST
SIST EN 60601-2-11:2015(Main)
Medical electrical equipment - Part 2-11: Particular requirements for basic safety and essential performance of gamma beam therapy equipment
EN 60601-2-11:2015

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of GAMMA
BEAM THERAPY EQUIPMENT, including MULTI-SOURCE STEREOTACTIC RADIOTHERAPY equipment,
hereafter referred to as ME EQUIPMENT.
If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to
ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the
case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.
HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS
within the scope of this standard are not covered by specific requirements in this standard
except in 7.2.13 and 8.4.1 of the general standard.

  • Standard
    53 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 62274:2006(Main)
Medical electrical equipment - Safety of radiotherapy record and verify systems
EN 62274:2005

This International Standard applies to the design and manufacture and some installation aspects of a RECORD AND VERIFY SYSTEM (RVS) for use in RADIOTHERAPY in human medical practice that a) provides, defines, or displays treatment machine set up data; imports data either through input by the OPERATOR or directly from other devices, b) may control the ability of that equipment to operate; c) records data of all TREATMENT sessions; and d) is intended to be: 1) for NORMAL USE, under the authority of appropriately licensed or QUALIFIED PERSONS, by OPERATORS having the required skills and training; 2) maintained in accordance with the recommendations given in the INSTRUCTIONS FOR USE; and 3) used within the environmental and electrical supply conditions specified in the technical description. This standard does not address dynamic beam deliveries. NOTE This may be addressed in a future version of this standard. It does, however, address certain specific aspects of the connection of the RVS to a network or to other radiotherapy equipment, and the communication protocol to be used.

  • Standard
    21 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 60601-2-68:2015/oprA1:2023(Amendment)
Amendment 1 - Medical electrical equipment - Part 2-68: Particular requirements for the basic safety and essential performance of X-ray-based image-guided radiotherapy equipment for use with electron accelerators, light ion beam therapy equipment and radionuclide beam therapy equipment
EN 60601-2-68:2015/prA1:2023
  • Draft
    49 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 60601-2-11:2015(Main)
Medical electrical equipment - Part 2-11: Particular requirements for basic safety and essential performance of gamma beam therapy equipment
EN 60601-2-11:2015

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of GAMMA
BEAM THERAPY EQUIPMENT, including MULTI-SOURCE STEREOTACTIC RADIOTHERAPY equipment,
hereafter referred to as ME EQUIPMENT.
If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to
ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the
case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.
HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS
within the scope of this standard are not covered by specific requirements in this standard
except in 7.2.13 and 8.4.1 of the general standard.

  • Standard
    53 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 62274:2006(Main)
Medical electrical equipment - Safety of radiotherapy record and verify systems
EN 62274:2005

This International Standard applies to the design and manufacture and some installation aspects of a RECORD AND VERIFY SYSTEM (RVS) for use in RADIOTHERAPY in human medical practice that a) provides, defines, or displays treatment machine set up data; imports data either through input by the OPERATOR or directly from other devices, b) may control the ability of that equipment to operate; c) records data of all TREATMENT sessions; and d) is intended to be: 1) for NORMAL USE, under the authority of appropriately licensed or QUALIFIED PERSONS, by OPERATORS having the required skills and training; 2) maintained in accordance with the recommendations given in the INSTRUCTIONS FOR USE; and 3) used within the environmental and electrical supply conditions specified in the technical description. This standard does not address dynamic beam deliveries. NOTE This may be addressed in a future version of this standard. It does, however, address certain specific aspects of the connection of the RVS to a network or to other radiotherapy equipment, and the communication protocol to be used.

  • Standard
    21 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
kSIST fprEN IEC 60601-2-57:2023(Main)
Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use
FprEN IEC 60601-2-57:2023

IEC 60601-2-57:2023 applies to basic safety and essential performance of equipment incorporating one or more sources of optical radiation in the wavelength range 200 nm to 3 000 nm, with the exception of laser radiation, and intended to create photobiological effects in humans for therapeutic, diagnostic, monitoring, and cosmetic or aesthetic applications; hereafter referred to as light source equipment (ls equipment).

  • Draft
    29 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 60601-2-68:2015/oprA1:2023(Amendment)
Amendment 1 - Medical electrical equipment - Part 2-68: Particular requirements for the basic safety and essential performance of X-ray-based image-guided radiotherapy equipment for use with electron accelerators, light ion beam therapy equipment and radionuclide beam therapy equipment
EN 60601-2-68:2015/prA1:2023
  • Draft
    49 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST-TP CEN/TR 12349:2023(Main)
Mechanical vibration - Guide to the health effects of vibration on the human body
CEN/TR 12349:2023

The aim of this CEN report is to provide information on the possible adverse health effects caused by exposure to vibration at work.  the report addresses manufacturers as well as employers and employees using vibrating machinery in order to improve their understanding of the possible health problems arising from occupational exposure to vibration.

  • Technical report
    17 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN ISO 80004-1:2023(Main)
Nanotechnologies - Vocabulary - Part 1: Core vocabulary (ISO 80004-1:2023)
EN ISO 80004-1:2023

This document defines core terms in the field of nanotechnology. This document is intended to facilitate communication between organizations and individuals in industry and those who interact with them.

  • Standard
    24 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    25 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN ISO 3262-4:2023(Main)
Extenders - Specifications and methods of test - Part 4: Whiting (ISO 3262-4:2022)
EN ISO 3262-4:2023

This document specifies requirements and corresponding methods of test for whiting.

  • Standard
    11 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    9 pages
    English language
    sale 10% off
    e-Library read for
    1 day