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Verathon BladderScan i10 User Manual

Verathon BladderScan i10
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81
Operations & Maintenance Manual: Product Specifications
0900‑5005 REV‑00
ELECTROMAGNETIC COMPATIBILITY
The system is designed to be in compliance with IEC 6060112, 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 facility.
The system complies with the applicable essential performance requirements specified in IEC 606011 and
606012‑37. 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 system, see “Essential Performance on page1.
ELECTROMAGNETIC EMISSIONS
Table 26. Guidance and Manufacturer’s DeclarationElectromagnetic 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 610003‑2
Class A
Voltage
fluctuations/flicker
emissions
IEC 61000‑3‑3
In compliance

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Verathon BladderScan i10 Specifications

General IconGeneral
BrandVerathon
ModelBladderScan i10
CategoryMedical Equipment
LanguageEnglish

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