Authorization Letter for Eurofins Product Service GmbH

QRI-CMSMART4GWW2_AutLet

This document is an authorization letter from BIOTRONIK SE & Co. KG, granting Eurofins Product Service GmbH the authority to act on their behalf in all matters relating to applications for equipment authorization with the Federal Communications Commission (FCC). The specific FCC ID covered by this authorization is QRI-CMSMART4GWW2.

The letter explicitly states that Eurofins Product Service GmbH is authorized to sign all documents related to these matters, and any actions taken by Eurofins on BIOTRONIK's behalf will have the same effect as if BIOTRONIK had taken those actions themselves. Furthermore, BIOTRONIK confirms their agreement to Eurofins' current valid General Terms and Conditions (AGB) and Testing and Certification Regulations (PZO), which are available on the Eurofins website. Finally, BIOTRONIK certifies that no party involved in this application is subject to a denial of benefits under Section 5301 of the Anti-Drug Abuse Act of 1988.


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tags: ["QRI-CMSMART4GWW2", "FCC ID", "Authorization", "Eurofins Product Service GmbH"]
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This document is an authorization letter from BIOTRONIK SE & Co. KG, granting Eurofins Product Service GmbH the authority to act on their behalf in all matters relating to applications for equipment authorization with the Federal Communications Commission (FCC). The specific FCC ID covered by this authorization is QRI-CMSMART4GWW2.

The letter explicitly states that Eurofins Product Service GmbH is authorized to sign all documents related to these matters, and any actions taken by Eurofins on BIOTRONIK's behalf will have the same effect as if BIOTRONIK had taken those actions themselves. Furthermore, BIOTRONIK confirms their agreement to Eurofins' current valid General Terms and Conditions (AGB) and Testing and Certification Regulations (PZO), which are available on the Eurofins website. Finally, BIOTRONIK certifies that no party involved in this application is subject to a denial of benefits under Section 5301 of the Anti-Drug Abuse Act of 1988.

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