Cena s DPH / bez DPH
Hlavní stránka>PD IEC/TR 62471-3:2015 Photobiological safety of lamps and lamp systems Guidelines for the safe use of intense pulsed light source equipment on humans
sklademVydáno: 2015-01-20
PD IEC/TR 62471-3:2015 Photobiological safety of lamps and lamp systems Guidelines for the safe use of intense pulsed light source equipment on humans

PD IEC/TR 62471-3:2015

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

Formát
Dostupnost
Cena a měna
Anglicky Zabezpečené PDF
K okamžitému stažení
7320 Kč
Čtěte normu po dobu 1 hodiny. Více informací v kategorii E-READING
Čtení normy
na 1 hodinu
732.00 Kč
Čtěte normu po dobu 24 hodin. Více informací v kategorii E-READING
Čtení normy
na 24 hodin
2196.00 Kč
Anglicky Tisk
Skladem
7320 Kč
Označení normy:PD IEC/TR 62471-3:2015
Počet stran:34
Vydáno:2015-01-20
ISBN:978 0 580 84356 3
Status:Standard
Popis

PD IEC/TR 62471-3:2015


This standard PD IEC/TR 62471-3:2015 Photobiological safety of lamps and lamp systems is classified in these ICS categories:
  • 31.260 Optoelectronics. Laser equipment
  • 29.140.01 Lamps in general

This part of IEC 62471, 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.