This document is a Covered Equipment Certification Attestation Letter from Lumicare Medtech Co., Ltd. It certifies that the equipment for which authorization is sought is not considered "covered" equipment, as prohibited by section 2.903 of the FCC rules. The letter further clarifies that if the equipment is produced by entities identified on the Covered List, an explanation is provided as to why the equipment is not "covered".
Additionally, Lumicare Medtech confirms that, as of the filing date, the company is not identified on the Covered List as an entity producing "covered" equipment. The attestation also states that the equipment does not include cybersecurity or anti-virus software produced or provided by Kaspersky Lab, Inc., or any of its successors and assignees, including equipment with integrated Kaspersky Lab software, in accordance with DA-24-886 and KDB 986446 D01 Covered Equipment Guidance section B(2a).
The document is signed by Tong Liu, R&D Manager of Lumicare Medtech Co., Ltd, and dated March 20, 2025. The FCC ID for the equipment is 2BM9Y0001.
Array
(
[0] => Array
(
[url_sha] => ee48cc2b9b15fe8508a29de941cfa6a9b0713d106de2ab2bf176fb7c46f2578a
[source] => fccid
[url] => https://apps.fcc.gov/eas/GetApplicationAttachment.html?id=8259796
[href_text] => Covered equipment list attestation
[href_description] => Lumicare Medtech Co., Ltd 0001 RFID Module 2BM9Y0001 2BM9Y0001 0001
[http_status] => 200
[http_lastmod] => 0000-00-00 00:00:00
[http_contenttype] =>
[http_filename] => GetApplicationAttachment.html?id=8259796
[http_size] => 27631
[file_sha256] => 02d32b719b714c7355ee2a596db04a6c8999ad5ae6bde3e2b3a46b0d95fd92b4
[domain] => document.fccid
)
)
Array
(
[file_sha256] => 02d32b719b714c7355ee2a596db04a6c8999ad5ae6bde3e2b3a46b0d95fd92b4
[cleanFccId] => 2BM9Y0001
[title] => Lumicare Medtech Covered Equipment Attestation Letter
[description] => Attestation letter certifying that Lumicare Medtech's equipment is not 'covered' under FCC rules and doesn't include Kaspersky software.
[brand_name] => Lumicare Medtech
[keywords] => ["2BM9Y0001", "Covered Equipment", "FCC Rules", "DA-24-886", "KDB 986446 D01"]
[intro] =>
This document is a Covered Equipment Certification Attestation Letter from Lumicare Medtech Co., Ltd. It certifies that the equipment for which authorization is sought is not considered "covered" equipment, as prohibited by section 2.903 of the FCC rules. The letter further clarifies that if the equipment is produced by entities identified on the Covered List, an explanation is provided as to why the equipment is not "covered".
Additionally, Lumicare Medtech confirms that, as of the filing date, the company is not identified on the Covered List as an entity producing "covered" equipment. The attestation also states that the equipment does not include cybersecurity or anti-virus software produced or provided by Kaspersky Lab, Inc., or any of its successors and assignees, including equipment with integrated Kaspersky Lab software, in accordance with DA-24-886 and KDB 986446 D01 Covered Equipment Guidance section B(2a).
The document is signed by Tong Liu, R&D Manager of Lumicare Medtech Co., Ltd, and dated March 20, 2025. The FCC ID for the equipment is 2BM9Y0001.
)
Array
(
[0] => Array
(
[id] => 8259796
[file_sha256] =>
[applicationId] => McurygyF4Uc4Nd6xMAgZZw==
[description] => Covered equipment list attestation
[shortTermConfidential] => No
[permanentConfidential] => No
[supercede] => No
[exhibitType] => Attestation Statements
[fileType] => Adobe Acrobat PDF
[displayType] => pdf
[fileSize] => 27633
[submissionDate] => 2025-05-02 00:00:00
[dateAvailable] => 2025-05-02 00:00:00
[creationDate] =>
[producer] =>
[modDate] =>
[title] =>
[creator] =>
[author] =>
[pages] =>
[realSize] =>
[html] => 0
[png] => 0
[txt] => 0
[version] => 1
[source] => 0
[fccId] => 2BM9Y0001
[cleanFccId] => 2BM9Y0001
[exif] => 0
)
)