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0900‑4868 REV‑08
ELECTROMAGNETIC COMPATIBILITY
The GlideScope BFlex system is designed to be in compliance with IEC 60601‑1‑2, which contains
electromagnetic compatibility (EMC) requirements for medical electrical equipment. The limits for emissions
and immunity specified in this standard are designed to provide reasonable protection against harmful
interference in a typical medical installation.
The system complies with the applicable essential performance requirements specified in IEC 60601‑1
and IEC 60601‑2‑18. Results of immunity testing show that the essential performance of the system is not
affected under the test conditions described in the following tables. For more information about the essential
performance of the GlideScope BFlex system, see
on page 1.
ELECTROMAGNETIC EMISSIONS
Table 19. Guidance and Manufacturer’s Declaration—Electromagnetic Emissions
The system is intended for use in the electromagnetic environment specified below. The customer or the user
of the system should ensure that it is used in such an environment.
EMISSIONS TEST
COMPLIANCE
ELECTROMAGNETIC ENVIRONMENT – GUIDANCE
RF emissions
CISPR 11
Group 1
The system uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to cause
any interference in nearby electronic equipment.
RF emissions
CISPR 11
Class A
The system is suitable for use in all establishments other than
domestic and those directly connected to the public low‑voltage
power supply network that supplies buildings used for domestic
purposes.
Harmonic emissions
IEC 61000‑3‑2
Class A
Voltage fluctuations/
flicker emissions
IEC 61000‑3‑3
In compliance
