Lasers and laser-related equipment - Test methods for laser-induced damage threshold - Classification of medical beam delivery systems

This document specifies a method of testing the laser-induced ignition and damage of medical beam delivery systems to allow checking of suitable products according to the classification system. NOTE 1 Take care when interpreting these results, since the direct applicability of the results of this test method to the clinical situation has not been fully established. NOTE 2 Users of products tested by this method are cautioned that the laser will be wavelength sensitive and tested at the wavelength for which it is intended to be used. If tested using other wavelengths, the power settings and modes of beam delivery need to be explicitly stated. CAUTION - This test method can involve hazardous materials, operations and equipment. This document provides advice on minimizing some of the risks associated with its use but does not purport to address all such risks. It is the responsibility of the user of this document to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use.

Lasers et équipements associés aux lasers — Méthodes d'essai du seuil d'endommagement provoqué par laser — Classification des systèmes de transmission de faisceau médical

General Information

Status
Published
Publication Date
11-Nov-2020
Current Stage
9092 - International Standard to be revised
Start Date
22-Dec-2025
Completion Date
27-Dec-2025

Relations

Effective Date
06-Jun-2022

Overview

ISO 22248:2020 specifies test methods and a classification system for the laser-induced ignition and damage threshold of medical beam delivery systems. It defines a repeatable laboratory procedure to assess whether products that transmit laser energy (e.g., optical fibres, articulated arms, hollow waveguides and applicators) are susceptible to ignition, flame spread or other damage when exposed to laser irradiation. The standard emphasises reproducible test conditions and cautions that results may not fully predict clinical outcomes. It also warns about hazardous operations and oxygen‑enriched atmospheres used in testing.

Key topics and technical requirements

  • Scope and purpose: Method for testing laser-induced ignition and damage of medical beam delivery systems and classifying test outcomes.
  • Test environments: Tests are carried out in ambient air and in oxygen‑enriched atmospheres (notably 60% ± 2% and up to 98% ± 2% oxygen) to simulate worst‑case clinical conditions.
  • Test types / classification:
    • Irradiation ignition (I) - ignition from external laser irradiation of the specimen.
    • Transmission ignition (T) - ignition caused by laser transmission through the specimen.
    • Transmission destruction (D) - non‑ignition damage (melting, crumbling, breaking) due to absorption during transmission.
  • Apparatus and setup: Requirements for a ventilated, draught‑resistant containment box, specimen holder/rack, laser source and beam delivery, power/energy meters, gas supply and oxygen control, smoke evacuation and environmental monitoring.
  • Specimen preparation and testing conditions: Specimens must be prepared per manufacturer instructions; variables (wavelength sensitivity, power settings, modes of delivery) must be explicitly stated when reporting results.
  • Safety considerations: CAUTION about hazardous materials, potential for intense fires (“rocket‑like” fire), toxic gases; responsibility on the user to establish safety and regulatory compliance.
  • Reporting: Standard requires documentation of test conditions and results to support classification.

Applications and who uses it

ISO 22248 is used by:

  • Manufacturers of medical laser fibres, applicators, handpieces and beam delivery systems for product development, risk assessment and labeling.
  • Independent test laboratories performing ignition and damage threshold testing for compliance and certification.
  • Regulatory and conformity assessment bodies evaluating safety of laser medical devices.
  • Clinical engineers and hospital procurement teams assessing device risks in oxygen‑rich clinical environments.
  • Product safety and quality teams validating designs to reduce laser‑induced fire hazards.

Relevant SEO keywords: ISO 22248, laser-induced damage threshold, medical beam delivery systems, laser ignition testing, oxygen-enriched atmosphere, laser safety, laser testing standards.

Related standards

  • ISO 13694 - Test methods for laser beam power (energy) density distribution
  • ISO/IEC Guide 99 - International vocabulary of metrology (VIM)
  • Referenced definitions from ISO 11810 and ISO 11145 are also used in ISO 22248.
Standard

ISO 22248:2020 - Lasers and laser-related equipment — Test methods for laser-induced damage threshold — Classification of medical beam delivery systems Released:11/12/2020

English language
18 pages
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Frequently Asked Questions

ISO 22248:2020 is a standard published by the International Organization for Standardization (ISO). Its full title is "Lasers and laser-related equipment - Test methods for laser-induced damage threshold - Classification of medical beam delivery systems". This standard covers: This document specifies a method of testing the laser-induced ignition and damage of medical beam delivery systems to allow checking of suitable products according to the classification system. NOTE 1 Take care when interpreting these results, since the direct applicability of the results of this test method to the clinical situation has not been fully established. NOTE 2 Users of products tested by this method are cautioned that the laser will be wavelength sensitive and tested at the wavelength for which it is intended to be used. If tested using other wavelengths, the power settings and modes of beam delivery need to be explicitly stated. CAUTION - This test method can involve hazardous materials, operations and equipment. This document provides advice on minimizing some of the risks associated with its use but does not purport to address all such risks. It is the responsibility of the user of this document to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use.

This document specifies a method of testing the laser-induced ignition and damage of medical beam delivery systems to allow checking of suitable products according to the classification system. NOTE 1 Take care when interpreting these results, since the direct applicability of the results of this test method to the clinical situation has not been fully established. NOTE 2 Users of products tested by this method are cautioned that the laser will be wavelength sensitive and tested at the wavelength for which it is intended to be used. If tested using other wavelengths, the power settings and modes of beam delivery need to be explicitly stated. CAUTION - This test method can involve hazardous materials, operations and equipment. This document provides advice on minimizing some of the risks associated with its use but does not purport to address all such risks. It is the responsibility of the user of this document to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use.

ISO 22248:2020 is classified under the following ICS (International Classification for Standards) categories: 31.260 - Optoelectronics. Laser equipment. The ICS classification helps identify the subject area and facilitates finding related standards.

ISO 22248:2020 has the following relationships with other standards: It is inter standard links to ISO 11432:2021. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

You can purchase ISO 22248:2020 directly from iTeh Standards. The document is available in PDF format and is delivered instantly after payment. Add the standard to your cart and complete the secure checkout process. iTeh Standards is an authorized distributor of ISO standards.

Standards Content (Sample)


INTERNATIONAL ISO
STANDARD 22248
First edition
2020-11
Lasers and laser-related equipment —
Test methods for laser-induced
damage threshold — Classification of
medical beam delivery systems
Lasers et équipements associés aux lasers — Méthodes d'essai du seuil
d'endommagement provoqué par laser — Classification des systèmes
de transmission de faisceau médical
Reference number
©
ISO 2020
© ISO 2020
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting
on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address
below or ISO’s member body in the country of the requester.
ISO copyright office
CP 401 • Ch. de Blandonnet 8
CH-1214 Vernier, Geneva
Phone: +41 22 749 01 11
Email: copyright@iso.org
Website: www.iso.org
Published in Switzerland
ii © ISO 2020 – All rights reserved

Contents Page
Foreword .iv
Introduction .v
1 Scope . 1
2 Normative references . 1
3 Terms and definitions . 1
4 Principle . 4
5 Significance and use of the test. 4
6 Apparatus . 4
6.1 General . 4
6.2 Containment box . 6
6.3 Specimen holder . 7
6.4 Lasers and beam delivery systems . 7
6.5 Power meter . 7
6.6 Gas supply system . 7
6.7 Environment . 8
6.7.1 Ambient air conditions . 8
6.7.2 Oxygen enriched atmospheres . 8
6.8 Smoke evacuation device . 8
7 Reagents and materials . 8
8 Preparation of test specimens . 9
9 Preparation of apparatus . 9
10 Test methods .10
10.1 General conditions .10
10.2 Testing during laser irradiation .10
10.3 Testing during laser transmission .11
11 Classification .12
11.1 General .12
11.2 Irradiation ignition testing (I) .13
11.3 Transmission ignition and destruction testing (T/D) .13
11.3.1 Transmission ignition testing (T) .13
11.3.2 Transmission destruction testing (D) .14
12 Test report .16
Bibliography .18
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out
through ISO technical committees. Each member body interested in a subject for which a technical
committee has been established has the right to be represented on that committee. International
organizations, governmental and non-governmental, in liaison with ISO, also take part in the work.
ISO collaborates closely with the International Electrotechnical Commission (IEC) on all matters of
electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/ directives).
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. ISO shall not be held responsible for identifying any or all such patent rights. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/ patents).
Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.
For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT) see www .iso .org/
iso/ foreword .html.
This document was prepared by Technical Committee ISO/TC 172, Optics and photonics, Subcommittee
SC 9, Laser and electro-optical systems.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/ members .html.
iv © ISO 2020 – All rights reserved

Introduction
Fire in an operating room is the most dangerous situation for patient and staff. Besides electrosurgical
devices and endoscopic light sources, even surgical lasers can be ignition sources for drapes, gowns
and tracheal tubes. This risk was identified very early and several ISO standards for laser proof
materials have been published. The medical beam delivery system itself, however, was out of focus.
Due to the increasing market on the one hand and necessity for cost reduction in health care on the
other hand fibres have come into the market with a risk of self-ignition of the core or cladding material.
Furthermore with reinvention of fibre-applicator-systems for contact application or integrated diffusor
systems they have an increased risk for self-ignition due to high absorption. This document elaborates
reproducible test parameters for medical beam delivery systems.
INTERNATIONAL STANDARD ISO 22248:2020(E)
Lasers and laser-related equipment — Test methods
for laser-induced damage threshold — Classification of
medical beam delivery systems
1 Scope
This document specifies a method of testing the laser-induced ignition and damage of medical beam
delivery systems to allow checking of suitable products according to the classification system.
NOTE 1 Take care when interpreting these results, since the direct applicability of the results of this test
method to the clinical situation has not been fully established.
NOTE 2 Users of products tested by this method are cautioned that the laser will be wavelength sensitive and
tested at the wavelength for which it is intended to be used. If tested using other wavelengths, the power settings
and modes of beam delivery need to be explicitly stated.
CAUTION — This test method can involve hazardous materials, operations and equipment. This
document provides advice on minimizing some of the risks associated with its use but does not
purport to address all such risks. It is the responsibility of the user of this document to establish
appropriate safety and health practices and to determine the applicability of regulatory
limitations prior to use.
2 Normative references
The following documents are referred to in the text in such a way that some or all of their content
constitutes requirements of this document. For dated references, only the edition cited applies. For
undated references, the latest edition of the referenced document (including any amendments) applies.
ISO 13694, Optics and photonics — Lasers and laser-related equipment — Test methods for laser beam
power (energy) density distribution
ISO/IEC Guide 99, International vocabulary of metrology — Basic and general concepts and associated
terms (VIM)
3 Terms and definitions
For the purposes of this document, the terms and definitions given in ISO/IEC Guide 99 and the
following apply.
ISO and IEC maintain terminological databases for use in standardization at the following addresses:
— ISO Online browsing platform: available at https:// www .iso .org/ obp
— IEC Electropedia: available at http:// www .electropedia .org/
3.1
afterflame
persistence of flaming of a material, under specified test conditions, after the ignition source has
been removed
[SOURCE: ISO 11810:2015, 3.1]
3.2
afterflame time
length of time for which a material continues to flame, under specified test conditions, after the ignition
source has been removed
[SOURCE: ISO 11810:2015, 3.2]
3.3
afterglow
persistence of glowing of a material, under specified test conditions, after cessation of flaming or, if no
flaming occurs, after the ignition source has been removed
[SOURCE: ISO 11810:2015, 3.3]
3.4
afterglow time
time during which a material continues to glow, under specified test conditions, after cessation of
flaming or, if no flaming occurs, after the ignition source has been removed
[SOURCE: ISO 11810:2015, 3.4]
3.5
beam diameter
d
diameter of a circular aperture in a plane perpendicular to the beam axis that contains 95 % of the total
beam power (energy)
[SOURCE: ISO 11145:2018, 3.3.1, modified — Value of contained total beam power set to 95 % and
Note 1 to entry removed.]
3.6
beam cross-sectional area
A
smallest completely filled area containing 95 % of the total beam power (energy)
[SOURCE: ISO 11145:2018, 3.6.1, modified — Value of contained total beam power set to 95 % and
Note 1 to entry removed.]
3.7
combustion
any continuing burning process that occurs in or on the specimen caused by a chemical process of
oxidation with the liberation of heat
EXAMPLE Flame, smouldering, rapid evolution of smoke.
[SOURCE: ISO 11810:2015, 3.7]
3.8
destruction
damage of the system during laser radiation transmission due to absorption rather than ignition
(crumbling, melting, disconnecting, breaking) with or without loss of parts of the system
3.9
flammable
subject to ignition and flaming combustion
[SOURCE: ISO 11810:2015, 3.9]
2 © ISO 2020 – All rights reserved

3.10
ignition
creation of combustion induced by the beam delivery of laser power
[SOURCE: ISO 11810:2015, 3.10, modified — "laser" was included before "power"]
3.10.1
irradiation ignition
ignition of a specimen by laser irradiation of the specimen from outside
3.10.2
transmission ignition
ignition of a specimen by a laser beam transmission through the specimen
3.11
laser resistance
measure of the ability of a material to withstand laser power without ignition or damage
[SOURCE: ISO 11810:2015, 3.11]
3.12
medical beam delivery system
product intended to transmit the laser beam from the source to the treatment site directly or by the use
of additional applicators
EXAMPLE Articulated arms, hollow waveguides, optical fibres.
Note 1 to entry: Directly means direct application either with bare fibres, shaped fibres or internal marked fibres.
3.12.1
applicator
attachment to the medical beam delivery system at the treatment site
EXAMPLE Focussing handpiece, micromanipulators, scanners, endoscopes, shaped tips like sapphire tips,
ceramic/metal tips, radial tips, focussing lenses or diffusor tips.
3.13
melting behaviour
softening of a material under the influence of heat (including shrinking, dripping and burning of molten
material, etc.)
[SOURCE: ISO 11810:2015, 3.12]
3.14
thermal resistance
ability of a material to resist conduction of heat
[SOURCE: ISO 11810:2015, 3.20]
3.15
product
finished medical device (samples)
3.16
reusable product
product intended to be prepared and re-sterilized for multiple use
[SOURCE: ISO 11810:2015, 3.16]
3.17
single use
product intended to be used once and then discarded
[SOURCE: ISO 11810:2015, 3.18]
4 Principle
WARNING — This test method can result in a rocket-like fire. Such a fire can produce intense
heat and light and toxic gases.
To simulate worst-case conditions, the material is exposed to laser power of known characteristics in
an environment up to 98 % ± 2 % oxygen.
5 Significance and use of the test
5.1 A medical beam delivery system is intended to transmit the laser beam from the source to the
treatment area. This can be articulated arms, hollow waveguides or optical fibres. It can deliver the
radiation to the target by connected applicators like focussing handpiece, micromanipulators, scanners
or endoscopes or fix mounted applicators as shaped tips like sapphire tips, ceramic/metal tips, radial
tips, focussing lenses or diffusor tips. Another technical solution is the direct application either with bare
fibres, shaped fibres or internal marked fibres.
5.2 This document describes a uniform and repeatable test method for measuring the laser-induced
ignition, flame spread and damage of medical beam delivery systems. Variables involved in laser ignition
have been fixed in order to establish a basis for comparison. This test method can be used to compare
different types and designs.
5.3 A large number and range of variables are involved in ignition. A change in one variable can affect
the outcome of the test. Caution should be observed, since the direct applicability of the results of this
test method to the clinical situation has not been fully established.
NOTE This method can be applied to study the effect of changing the test conditions, but this is outside the
scope of this document. For example, variation of the breathing-gas flow rate or different breathing-gas mixtures
might affect the laser ignition.
5.4 Since an oxygen-enriched atmosphere is often present in the clinical situation, either intentionally
or unintentionally, the test is performed under ambient air conditions and an environment of 60 % ± 2%
and 98 % ± 2 % oxygen, respectively.
5.5 The preparation of the specimen shall be in accordance with the manufacturer's instructions for use.
6 Apparatus
6.1 General
The test apparatus shall consist of a draught-resistant ventilated containment box, specimen holder,
specimen rack, laser energy source and associated parts (see Figures 1 and 2).
4 © ISO 2020 – All rights reserved

Key
1 medical beam delivery system 6 flashback arrestor
2 medical beam delivery system support using two clamps 7 oxygen flow meter and controller
3 laser source for irradiation 8 pressure regulator with inlet and outlet
gauges
4 containment box (lateral view) 9 quick-action inert gas valve
5 enclosure cover (may be multi-piece) 10 opening for laser access
11 liquid for cooling/cleaning
Figure 1 — Apparatus for irradiation ignition testing
Key
1 medical beam delivery system 6 flashback arrestor
2 medical beam delivery system support using two clamps 7 oxygen flow meter and controller
3 laser source for transmission 8 pressure regulator with inlet and outlet
gauges
4 containment box (lateral view) 9 quick-action inert gas valve
5 enclosure cover (may be multi-piece) 10 opening for laser access
11 liquid for cooling / cleaning
Figure 2 — Apparatus for transmission ignition testing
6.2 Containment box
The containment box controls the environment around the specimen while allowing the laser beam to
be directed onto the specimen.
The containment box shall
a) be rectangular in shape and have dimensions of approximately 46 cm × 46 cm × 46 cm,
b) be fire-proof and easily cleaned of soot and residue from burned specimens,
c) allow the mounting of the test specimen for the irradiation of the specimen (Figure 1) and
transmitted irradiation (Figure 2),
d) allow access to the specimen,
e) allow direct access of the laser beam to the specimen (Figure 1),
6 © ISO 2020 – All rights reserved

f) allow observation with video cameras on the top and on all sides of the box; a minimum of three
video cameras (one camera positioned above the containment box and two cameras positioned at
two of the sides of the containment box) is needed for recording purposes,
g) exhaust the gas and any products of combustion to a safe area,
h) allow cleaning of the box, and cleaning of the covers and/or windows themselves,
i) be capable of maintaining an environment of 60 % ± 2% and 98 % ± 2% respectively oxygen around
the specimen,
j) allow to be rapidly flooded with nitrogen or another gas to extinguish any fire inside the box, and
k) have internal surfaces that are non-reflective to protect the specimen from reflections.
Other configurations may be used, as long as the requirements of the test method as defined herein are
not affected.
6.3 Specimen holder
The specimen holder shall consist of suitable material and construction which allows the passage of the
medical beam delivery system. The specimen shall be positioned within the specimen holder in such a
way that the end of the fibre, specifically the connection between fibre and end piece, is a minimum of
3 cm away from the specimen holder.
6.4 Lasers and beam delivery systems
WARNING — Surgical lasers emit radiation of sufficient power to damage living tissue or ignite
fires directly or by reflection of radiation. In addition to other precautions, test personnel
should be trained in the use of lasers and take proper safety measures based on the type of laser
being used. These precautions should
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ISO 22248:2020 is a standard that provides a method for testing the ignition and damage of medical beam delivery systems caused by lasers. The purpose of this test is to classify suitable products according to a classification system. However, it should be noted that the direct applicability of the test results to the clinical setting has not been fully established. The document warns users that the laser's effectiveness is dependent on the intended wavelength and, if tested using other wavelengths, the power settings and modes of beam delivery must be specified. It is important to note that this test method involves hazardous materials, operations, and equipment. While the document offers advice on minimizing risks, it is not comprehensive and the responsibility falls on the user to establish appropriate safety measures and determine regulatory limitations before conducting tests.

제목: ISO 22248:2020 - 레이저 및 레이저 관련 장비 - 레이저 유도 파손 임계값 시험 방법 - 의료 빔 전달 시스템 분류 내용: 이 문서는 의료 빔 전달 시스템의 레이저 유도 발화 및 손상을 테스트하기 위한 방법을 규정하며, 분류 체계에 따라 적합한 제품을 확인할 수 있도록 합니다. 참고 1: 이러한 결과를 해석할 때는 실제 임상 상황에 이러한 테스트 방법의 결과를 직접적으로 적용하는 것에 주의해야 합니다. 참고 2: 이 방법으로 테스트된 제품을 사용하는 사용자는 레이저가 특정 파장에서 작동하도록 테스트되며, 다른 파장을 사용하여 테스트하는 경우 전원 설정 및 빔 전달 모드를 명확하게 명시해야합니다. 주의: 이 테스트 방법은 위험한 물질, 운영 및 장비를 포함할 수 있습니다. 이 문서는 이러한 사용하는 우려에 대한 일부 위험을 최소화하기 위한 안내를 제공하지만 모든 위험을 다루지는 않습니다. 이 문서의 사용자는 적절한 안전 및 보건 관행을 수립하고 사용 전 규제 제한의 적용 가능 여부를 결정하는 것이 사용자의 책임입니다.

記事のタイトル:ISO 22248:2020 - レーザーおよびレーザー関連機器- レーザー誘起損傷閾値のテスト方法- 医療用ビームデリバリーシステムの分類 記事の内容:この文書は、適切な製品を分類システムに従って確認するための医療用ビームデリバリーシステムのレーザー誘起着火および損傷のテスト方法を規定しています。注意事項1:このテスト方法の結果を解釈する際には注意が必要です。なぜなら、このテスト方法の結果を臨床的な状況に直接適用することが完全に確立されていないからです。注意事項2:この方法でテストされた製品を使用するユーザーは、レーザーが波長に敏感であり、使用する波長でテストされていることに注意する必要があります。他の波長でテストする場合、出力設定とビームデリバリーモードを明示する必要があります。注意-このテスト方法には、有害な物質、操作、および設備が関与する場合があります。この文書はその使用に関連する一部のリスクを最小限に抑えるためのアドバイスを提供しますが、すべてのリスクを網羅しているわけではありません。したがって、この文書の使用者は、適切な安全衛生慣行を確立し、使用する前に規制制限の適用性を決定する責任を負います。

제목: ISO 22248:2020 - 레이저 및 레이저 관련 장비에 대한 시험 방법 - 의료용 광선 전달 시스템의 레이저 유발 손상 임계치의 분류 내용: 이 문서는 적절한 제품을 분류 시스템에 따라 확인할 수 있도록 의료용 광선 전달 시스템의 레이저 유발 발화 및 손상 테스트 방법을 명시하고 있습니다. 주의 1 이러한 결과를 해석할 때, 이 테스트 방법의 결과를 임상 상황에 직접 적용하는 것은 완전히 확립되지 않았으므로 주의해야 합니다. 주의 2 이 방법으로 테스트된 제품을 사용하는 사용자는 레이저가 파장에 민감하며, 사용하려는 파장에서 테스트되었을 것입니다. 다른 파장으로 테스트한 경우, 전력 설정 및 광선 전달 모드를 명확히 명시해야 합니다. 주의 - 이 테스트 방법은 위험한 물질, 작업 및 장비를 포함할 수 있습니다. 이 문서는 사용 시 이러한 위험을 최소화하기 위한 조언을 제공하지만, 모든 위험을 다루지는 않습니다. 테스트 방법을 사용하기 전에 적절한 안전 및 보건 관행을 수립하고 규제 제한의 적용 가능성을 결정하는 것은 사용자의 책임입니다.

記事のタイトル:ISO 22248:2020 - レーザーおよびレーザー関連機器 - レーザー誘起ダメージのしきい値に関する試験方法 - 医療用ビームデリバリーシステムの分類 記事の内容:本文書は、医療用ビームデリバリーシステムにおけるレーザーによる誘起点火およびダメージのテスト方法を定め、分類システムに基づいて適切な製品を確認するためのものです。注意1:これらの結果を解釈する際は注意が必要であり、このテスト方法の結果を臨床の状況に直接適用することが完全に確立されていないことに留意する必要があります。注意2:この方法でテストされた製品の使用者は、レーザーが使用を意図されている波長でテストされており、他の波長でテストする場合は、電力設定とビームデリバリーモードを明示する必要があります。注意:このテスト方法には、危険な材料、操作、および装置が関与する場合があります。本文書はその使用に伴う一部のリスクを最小限に抑えるための助言を提供しますが、すべてのリスクに対処しているわけではありません。本文書の使用者は、適切な安全衛生規定を確立し、使用前に規制制限の適用可能性を確認する責任があります。

The article discusses ISO 22248:2020, which is a standard that provides a method for testing the laser-induced ignition and damage of medical beam delivery systems. The purpose of this test is to determine if the products meet the classification system requirements. However, it is important to note that the applicability of these test results to clinical situations has not been fully established. Users of products tested by this method should be aware that the laser is wavelength sensitive and should be tested at the intended wavelength. If tested at different wavelengths, the power settings and modes of beam delivery must be specified. It is also emphasized that this test method involves hazardous materials, operations, and equipment. While the document offers advice on minimizing risks, it does not cover all potential risks. Therefore, it is the responsibility of the user to establish appropriate safety and health practices and determine regulatory limitations before using the test method.