This document is an agent authorization letter from Shenzhen Raycome Health Technology Co., Ltd. to the Federal Communications Commission (FCC). It authorizes Eurofins Product Service GmbH to act on behalf of Shenzhen Raycome Health Technology Co., Ltd. in all matters relating to applications for equipment authorization, including the signing of all documents related to these matters.
The FCC ID for the equipment authorization is [2BLMA-AUTO002]. Shenzhen Raycome Health Technology Co., Ltd. confirms that any and all acts carried out by Eurofins Product Service GmbH on their behalf shall have the same effect as acts of their own.
By signing this application form, Shenzhen Raycome Health Technology Co., Ltd. agrees to Eurofins' current valid General Terms and Conditions (AGB), Testing and Certification Regulations (PZO), which can be viewed on the website www.eurofins.de/ee or retrieved on request. They also certify that no party to this application is subject to a denial of benefits, including FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 862.
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The FCC ID for the equipment authorization is [2BLMA-AUTO002]. Shenzhen Raycome Health Technology Co., Ltd. confirms that any and all acts carried out by Eurofins Product Service GmbH on their behalf shall have the same effect as acts of their own.
By signing this application form, Shenzhen Raycome Health Technology Co., Ltd. agrees to Eurofins' current valid General Terms and Conditions (AGB), Testing and Certification Regulations (PZO), which can be viewed on the website www.eurofins.de/ee or retrieved on request. They also certify that no party to this application is subject to a denial of benefits, including FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 862.
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