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PD IEC/TR 62471-3:2015

Current

Current

The latest, up-to-date edition.

Photobiological safety of lamps and lamp systems Guidelines for the safe use of intense pulsed light source equipment on humans

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

20-01-2015

€254.76
Excluding VAT

FOREWORD
INTRODUCTION
1 Scope and object
2 Normative references
3 Terms and definitions
4 Responsibility for safe working conditions
5 Risks from exposure to IPL optical radiation
6 Causes of risks
7 Risk assessment
8 Education and training
Annex A (informative) - Biological effects, SKIN TYPES
Annex B (informative) - Personal eye protection
Annex C (informative) - IPL technology, classification
Annex D (informative) - Warning sign
Annex E (informative) -
Bibliography

Gives guidelines for the safe use of INTENSE PULSED LIGHT (IPL) source equipment in professional premises.

Committee
EPL/76
DocumentType
Standard
Pages
34
PublisherName
British Standards Institution
Status
Current

This part of IEC62471, which is a technical report, provides guidelines for the safe use of INTENSE PULSED LIGHT (IPL) source equipment in professional premises.

This technical report sets out the control measures recommended for the safety of recipients of IPL treatment, staff, service, maintenance personnel and others. Engineering controls which form part of the IPL equipment or the installation are also briefly described to provide an understanding of the general principles of protection.

1.2 Object

The object of this report is to provide information which helps to protect persons from hazardous exposure to optical radiation and other associated hazards by providing guidance on how to establish safety measures and procedures.

NOTE Although the manufacturers provide treatment information in their instructions for use, such information may not be exhaustive or applicable to all CLIENT treatment conditions.

If IPLs are applied to patients in medical premises, the physician is deemed to be responsible for all medical aspects of the treatment including his or her decisions about questions of indication and contraindication such as found in Clauses 5 and 6.

Standards Relationship
IEC TR 62471-3:2015 Identical

IEC 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

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