Calibration Verification Procedure; Disposal; Contraindications; Product Features - B.O.L.T BT4 User Manual

B.O.L.T User Manual

5.5 Calibration Verification Procedure

This calibration verification procedure, technical descriptions, circuit diagrams, component
part lists and assembly instructions are restricted to access by the responsible service
personnel and is not applicable in normal usage.

5.6 Disposal

Dispose the device, accessories, and consumables according to local disposal and recycling
laws.
This symbol is applicable for EU member countries only.
To avoid potential negative consequences for the environment and possibly human health,
care should be taken while disposing of (i) for EU member countries - in accordance with
WEEE (Directive on Waste Electrical and Electronic Equipment), or (ii) for all other countries,
in accordance with local disposal and recycling laws.

The probe cover need to be disposed after the single use to avoid cross-
contamination.

The probe cover disposal after use should adhere to the local authority
guidelines/norms.

6. Contraindications

not recommended for people with serious arrhythmia, patients implanted
The B.O.L.T device is
with an electrical device, patients with preeclampsia, atrial fibrillation, peripheral arterial
disease, and patients undergoing intravascular therapy or arterio-venous shunt or people
who received a mastectomy. Consult your doctor during pregnancy, arrhythmia, and
arteriosclerosis. The analyzed results from the devices are not sufficient to make a correct
diagnosis of the patient`s clinical condition. A detailed clinical history of the patient
with the results of any other tests suggested by a doctor is also required.
contraindicated for any person who is connected to a wearable or implantable electronic
device or instrument, such as a pacemaker or defibrillator. This device is not intended to be a
diagnostic device. Contact your physician if any abnormal values are indicated. Do not use
the device in an MR environment, in an explosive atmosphere, or on neonatal patients. This
device is not defibrillation proof per IEC 60601-1.

7. Product Features

 Elegant design enables simple and easy use of the product.
 Multiple Platform Support and same application for multiple users.
 Secured Cloud application to share and manage trends with health data.
© Copyright 2019, All Rights Reserved. AmZetta Technologies Private Ltd.
together
This device is
17