iTeh StandardsiTeh Standards
EURUSD
Your shopping cart is empty.
SIST

SIST EN 60601-2-22:1995

(Main)

Medical electrical equipment -- Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment

Medical electrical equipment -- Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment

EN following parallel vote * Superseded by EN 60601-2-22:1996

Medizinische elektrische Geräte -- Teil 2: Besondere Festlegungen für die Sicherheit von diagnostischen und therapeutischen Lasergeräten

Appareils électromédicaux -- Partie 2: Règles particulières de sécurité pour les appareils thérapeutiques et de diagnostic à laser

Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment (IEC 601 2 22:1992)

General Information

Status
Withdrawn
Publication Date
30-Apr-1995
Withdrawal Date
30-Jun-2001
ICS
11.040.55 - Diagnostic equipment
11.040.60 - Therapy equipment
Technical Committee
IEMO - Electrical equipment in medical practice
Current Stage
9900 - Withdrawal (Adopted Project)
Start Date
01-Jul-2001
Due Date
01-Jul-2001
Completion Date
01-Jul-2001
Ref Project
EN 60601-2-22:1992 - Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment

Relations

Replaced By
SIST EN 60601-2-22:2001 - Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment (IEC 60601-2-22:1995)
Effective Date
01-Jul-2001
Replaced By
SIST EN 60601-2-22:2001 - Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment (IEC 60601-2-22:1995)
Effective Date
29-Jan-2023
Replaced By
SIST EN 60601-2-22:2001 - Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment (IEC 60601-2-22:1995)
Effective Date
07-Jun-2022

Buy Standard

EN 60601-2-22:1995EN 60601-2-22:1995
PreviousNext
Standard
EN 60601-2-22:1995
English language
25 pages
sale 10% off
Preview
sale 10% off
Preview
e-Library read for
1 day

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 60601-2-22:1995
01-maj-1995
Medical electrical equipment - Part 2: Particular requirements for the safety of
diagnostic and therapeutic laser equipment (IEC 601 2 22:1992)
Medical electrical equipment -- Part 2: Particular requirements for the safety of diagnostic
and therapeutic laser equipment
Medizinische elektrische Geräte -- Teil 2: Besondere Festlegungen für die Sicherheit von
diagnostischen und therapeutischen Lasergeräten
Appareils électromédicaux -- Partie 2: Règles particulières de sécurité pour les appareils
thérapeutiques et de diagnostic à laser
Ta slovenski standard je istoveten z: EN 60601-2-22:1992
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
11.040.60 Terapevtska oprema Therapy equipment
SIST EN 60601-2-22:1995 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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

SIST EN 60601-2-22:1995

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

SIST EN 60601-2-22:1995

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

SIST EN 60601-2-22:1995

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

SIST EN 60601-2-22:1995

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

SIST EN 60601-2-22:1995

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

SIST EN 60601-2-22:1995

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

SIST EN 60601-2-22:1995

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

SIST EN 60601-2-22:1995

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

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 IEC 60601-2-22:2020(Main)
Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment
EN IEC 60601-2-22:2020

This part of IEC 60601 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of laser
equipment for surgical, therapeutic, medical diagnostic, cosmetic or veterinary applications,
intended for use on humans or animals, classified as LASER PRODUCT of CLASS 1C where the
ENCLOSED LASER is of CLASS 3B or 4, or CLASS 3B, or CLASS 4.
MEDICAL ELECTRICAL EQUIPMENT or MEDICAL ELECTRICAL SYSTEMS which incorporate lasers as
sources of energy being transferred to the PATIENT or animal and where the lasers are
specified as above, are referred to as “laser equipment” in this document.
NOTE 1 LASER PRODUCTS for these applications classified as a Class 1, Class 1M, CLASS 2, Class 2M or
CLASS 3R LASER PRODUCT, are covered by IEC 60825-1:2014 and by the general standard.
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 to ME EQUIPMENT and to ME SYSTEMS, as relevant.
Hazards inherent in the intended physiological function of laser equipment within the scope of
this document are not covered by specific requirements in this document except in 7.2.13,
Physiological effects, of the general standard.

  • Standard
    33 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 60601-2-22:2013
Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, therapeutic and diagnostic laser equipment
EN 60601-2-22:2013

This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of laser equipment for either surgical, therapeutic, medical diagnostic, cosmetic, or veterinary applications, intended for its use on humans or animals, classified as a CLASS 3B or CLASS 4 LASER PRODUCT as defined by 3.22 and 3.23 in IEC 60825-1, hereafter referred to as LASER EQUIPMENT. Throughout this International Standard, light emitting diodes(LED) are included whenever the word “laser” is used.
NOTE 1 Refer to Definition 3.49 in IEC 60825-1.
NOTE 2 Laser products for these applications classified as a CLASS 1, 1M, 2, 2M or CLASS 3R LASER PRODUCT, are covered by IEC 60825-1 and IEC 60601-1. 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. HAZARD inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specifi requirements in this standard except in 7.2.13 and 8.4.1 of the General Standard. NOTE See also 4.2 of the General Standard. This standard can also be applied to surgical, cosmetic, therapeutic and diagnostic laser equipment used for compensation or alleviation of disease, injury o disability.

  • Standard
    31 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN 60601-2-57:2011
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 (IEC 60601-2-57:2011)
EN 60601-2-57:2011

This International Standard 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 non-visual photobiological effects in humans or animals for therapeutic, diagnostic, monitoring, cosmetic/aesthetic or veterinary applications; hereafter referred to as light source equipment (LS EQUIPMENT).
This particular standard does not apply to equipment for sun tanning, for ophthalmic instruments or for infant phototherapy.
NOTE Safety requirements in this particular standard are intended to address only HAZARDS to the eye and skin; hazards to internal tissues are not included in its scope.
LS EQUIPMENT may consist of a single or multiple sources of OPTICAL RADIATION, with or without power supply, or may be incorporated into a complex system that includes optical, electrical or mechanical systems or sources of other radiation.
NOTE Annexes AA to EE have been included for purposes of general guidance and to illustrate many typical cases. However, the annexes should not be regarded as definitive or exhaustive.

  • Standard
    40 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-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 3262-22:2023(Main)
Extenders - Specifications and methods of test - Part 22: Flux-calcined kieselguhr (ISO 3262-22:2023)
EN ISO 3262-22:2023

This document specifies requirements and corresponding methods of test for flux-calcined kieselguhr.

  • Standard
    11 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    8 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN ISO 18473-4:2023(Main)
Functional pigments and extenders for special applications - Part 4: Nanoscale titanium dioxide for photocatalytic application (ISO 18473-4:2022)
EN ISO 18473-4:2023

This document specifies requirements and corresponding test methods for nanoscale titanium dioxide (TiO2) in either powder or suspension form for photocatalytic application.
This document is applicable to modified nanoscale titanium dioxide for photocatalytic application. Such modification can be surface treatment, coating, doping and combination thereof.

  • Standard
    13 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    10 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN ISO 3262-3:2023(Main)
Extenders - Specifications and methods of test - Part 3: Blanc fixe (ISO 3262-3:2023)
EN ISO 3262-3:2023

This document specifies requirements and corresponding methods of test for blanc fixe.

  • Standard
    14 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    10 pages
    English language
    sale 10% off
    e-Library read for
    1 day
SIST
SIST EN IEC 63044-4:2021/AC:2023(Corrigendum)
Home and building electronic systems (HBES) and building automation and control systems (BACS) - Part 4: General functional safety requirements for products intended to be integrated in HBES and BACS
EN IEC 63044-4:2021/AC:2023-07
  • Corrigendum
    1 page
    English language
    sale 10% off
    e-Library read for
    1 day