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Laser product classification

Standards compliance

The 1675 LambdaUnite MSS product complies with the applicable IEC standards and the

Food and Drug Administration's Center for Devices and Radiological Health

(FDA/CDRH) regulations.

FDA/CDRH regulations

Laser products are classified in accordance with the FDA/CDRH - 21 CFR 1010 and 1040

standards. The classification scheme is based on the ability of the laser emission to cause

injury to eye or skin during normal operating conditions.

In the United States, lasers and laser systems in the infrared wavelength range (greater

than 700 nm) are assigned to one of the following classes (please also refer to the section

"FDA/CDRH laser classification"

•

Class I,

•

Class IIIb or

•

Class IV.

Laser classification is dependent upon operating wavelength, output power and fiber mode

field diameter (core diameter).

IEC requirements

The International Electro-Technical Commission (IEC) establishes standards for the

electrical and electronic industries. The international standards IEC 60825-Part 1 and 2

have been established for the worldwide safety of laser products.

According to the IEC classification, lasers and laser systems in the infrared wavelength

range (greater than 700 nm) are assigned to one of the following classes (please also refer

to the section

•

Class 1,

•

Class 1M,

•

Class 3R,

•

Class 3B, or

•

Class 4.

1675 LU MSS

365-374-159R11.01.28 Release 11.01.28

Issue 1 November 2012

(1-18)):

"IEC laser classification"

(1-18)):

1 - 1 7

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Este manual también es adecuado para:

Lambdaunite

Laser Product Classification - Alcatel-Lucent 1675 Manual De Seguridad

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