This document presents the RF Exposure Report for the PANDA free Intraoral Digital Impression Instrument, manufactured by Ziyang Freqty Medical Equipment Co., Ltd. The report, identified by number SZCR240800338404, assesses the device's compliance with FCC radiofrequency radiation exposure limits as outlined in FCC Rules 47 CFR §2.1091 and KDB 447498 D04 interim General RF Exposure Guidance v01.
The evaluation considers various exemption methods, including blanket exemptions, MPE-based exemptions, and SAR-based exemptions, to determine if the device meets the required safety standards. Testing was conducted between November 27, 2024, and January 15, 2025, with the report issued on January 18, 2025. The results indicate that the EUT complies with the specified standards, ensuring safe operation within established RF exposure limits. The device is deemed to qualify for SAR test exemption, making this report a substitute for a full SAR assessment.
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This document presents the RF Exposure Report for the PANDA free Intraoral Digital Impression Instrument, manufactured by Ziyang Freqty Medical Equipment Co., Ltd. The report, identified by number SZCR240800338404, assesses the device's compliance with FCC radiofrequency radiation exposure limits as outlined in FCC Rules 47 CFR §2.1091 and KDB 447498 D04 interim General RF Exposure Guidance v01.
The evaluation considers various exemption methods, including blanket exemptions, MPE-based exemptions, and SAR-based exemptions, to determine if the device meets the required safety standards. Testing was conducted between November 27, 2024, and January 15, 2025, with the report issued on January 18, 2025. The results indicate that the EUT complies with the specified standards, ensuring safe operation within established RF exposure limits. The device is deemed to qualify for SAR test exemption, making this report a substitute for a full SAR assessment.
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