Please read all following instructions, precautions, and warnings carefully before use.

Indications for Use

The Cardiovascular Suite is a software program that is intended to aid trained healthcare practitioners in the quantitative analysis of vascular ultrasound images in adults, particularly for the measurement of the diameter and its changes on the brachial artery, the diameter and its changes on the carotid artery, the Carotid Intima-Media Thickness, and for carotid plaque analysis.

Contraindications 

The Cardiovascular Suite device is not intended for use as a test that provides a direct diagnosis of any cardiovascular disease. It is intended to supplement, not substitute, the physician’s decision-making process for diagnosis and treatment. It should be used in conjunction with knowledge of the patient’s history and other clinical findings.

Precautions and Warnings

Below are a list of Precautions and Warnings for the Cardiovascular Suite. All of the following items are found in their appropriate sections throughout this document as well.

Precautions

Warnings

Lifetime

The product lifetime is 2 years from the software build date. In this period, Quipu will provide security updates.

Labeling

The product labeling for the Cardiovascular Suite is comprised of the Manual and Instructions for Use, the login screen of the software as well as in the product license key, and product package leaflets.

Below is a table of all labeling symbols for the Cardiovascular Suite.

Labeling Symbols Table

Symbol

Meaning

Prescription Only: Caution: U.S Federal law restricts this device to sale by or on the order of a physician or health care practitioner.

Indicates the item is a medical device.

Unique Device Identification

Manufacturer information.

Year of Manufacture.

Caution. Indicates the need for the user to consult the instructions for use for important cautionary information such as warnings and precautions that cannot, for a variety of reasons, be presented on the medical device itself.

Consult instructions for use.

CE Mark (Conformité Européenne).

The product is in compliance with the legal requirements of the European Regulation (EU) 2017/745 for medical devices.

Do not store below 5ºC or above 55ºC.

Do not store below 5% humidity or above 95% humidity.