OPERATIONAL INSTRUCTIONS

Corcym Device Tracking System

In alignment with our effort for continuous improvement of our products and services, as of March 2^nd 2023, a Device Tracking System will be available at the following address http://devicetracking.corcym.com/ for the submission of Device Tracking Forms to Corcym.

As a manufacturer of medical devices in scope of USA Title 21 Code of Federal Regulations (CFR) Part 821 and Canada SOR/98-282 (art.54, 67, 68), Corcym is required to maintain an effective tracking system to promptly locate devices distributed in USA and Canada.

The system will replace the current paper Patient Registration Forms, which are handwritten and mailed to Corcym. It will also allow you to access all your device records at any time and provide additional functionalities, like the possibility to download Patient Cards.

To gain access to the system, please send a request for account activation to customer.qualityhv@corcym.com from a general department e-mail (preferred) or your professional e-mail, specifying the name and address of your institution as well as your department.

As soon as your account is activated, you will receive an e-mail by Microsoft on behalf of CORCYM with the request to “accept the invitation.” We encourage you to complete the registration process by March 31^st 2023.

A dedicated guide, including comprehensive Operational Instructions, is available to support you in the registration process and with system usage.

For questions or further clarification, please refer to your Corcym representative.
Sincerely,

Laura Mannino
Customer Quality Manager

CC-MK-001118 B

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