Test Report

Test Result Certification

Testing Information

1 General Description

1.1 Description of the EUT

RF specification:

1.2 Description of test modes

All the test modes were carried out with the EUT in normal operation, the final test mode of the EUT was the worst test mode for emission test, which was shown in this report and defined as:

1.3 Description of support units

The EUT has been tested as an independent unit together with other necessary accessories or support units. The following support units or accessories were used to form a representative test configuration during the tests.

Support equipment list

Support cable list

2 Measurement uncertainty

This uncertainty represents an expanded uncertainty expressed at approximately the 95% confidence level using a coverage factor of k=2.

3 Test facilities and accreditations

3.1 Test laboratory

4 List of test equipment

Software version: 2.6

5 Test result

5.1 Requirement

§1.1310: The criteria listed in the following table shall be used to evaluate the environment impact of human exposure to radio frequency (RF) radiation as specified in §1.1307(b), except in the case of portable devices which shall be evaluated according to the provisions of FCC part 2.1093 of this chapter.

Table 1 to §1.1310(e)(1) - Limits for Maximum Permissible Exposure (MPE)

f = frequency in MHz

* = Plane-wave equivalent power density

Note 1: Occupational/controlled exposure limits apply in situations in which persons are exposed as a consequence of their employment provided those persons are fully aware of the potential for exposure and can exercise control over their exposure. Note 2: General population/uncontrolled exposure limits apply in situations in which the general public may be exposed, or in which persons who are exposed as a consequence of their employment may not be fully aware of the potential for exposure or cannot exercise control over their exposure.

5.2 Test setup

The RF exposure test was performed in anechoic chamber.

Diagram description: A diagram shows the EUT (Equipment Under Test) centrally placed. Around it, at a distance of 20cm, are labels for 'Left', 'Right', 'Front', 'Rear', 'Bottom', and 'Z axis'. A device labeled 'MAGPY-8H3D+ED3' is shown to the right.

5.3 Test Procedures

• The RF exposure test was performed in anechoic chamber.
• E and H-field measurements should be made with these devices considered to meet the § 2.1091-Mobile conditions ("generally be used in such a way that a separation distance of at least 20 centimeters is normally maintained between the RF source's radiating structure(s) and [the nearest person]").
• The highest emission level was recorded and compared with limit.
• The EUT was measured according to the dictates of KDB 680106 D01 Wireless Power Transfer v04.

5.4 Information of test equipment

Test equipment: MAGPy-8H3D+ED3

• Diameter: 60mm
• 8 isotropic H-field sensors: Concentric loops of 1cm² arranged at the corner of a cube of 22mm side length
• 1 isotropic E-field sensor: Orthogonal dipole/monopple(arm length:50mm)
• Measurement center: 18.5mm from the probe tip
• Dimensions: 110*635*35mm (MAGPy-8H3D+E3D V2 & MAGPy-DAS V2)

Textual description of image: A close-up view of a test probe, without its casing, showing intricate wiring and sensor components.

5.5 Test results

Test condition 1: Mode 4 operating mode with client device (1 % battery status of client device)

Test condition 2: Mode 4 operating mode with client device (50 % battery status of client device)

Test condition 3: Mode 4 operating mode with client device (99 % battery status of client device)

Photographs of the Test Setup

See the Appendix - Test Setup Photos.

Photographs of the EUT

See the Appendix - EUT Photos.

Statement

1. This report is invalid without the seal and signature of the laboratory.
2. The test results of this report are only responsible for the samples submitted. Client shall be responsible for representativeness of the sample and authenticity of the material.
3. The report shall not be partially reproduced without the written consent of the Laboratory.
4. This report is invalid if transferred, altered or tampered with in any form without authorization.
5. The observations or tests with special mark fall outside the scope of accreditation, and are only used for purpose of commission, research, training, internal quality control etc.
6. Any objection to this report shall be submitted to the laboratory within 15 days from the date of receipt of the report.

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