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SFGHPOCT.orgPOCT Attestation Page Hemochron Jr. Signature Elite Activated Clotting Time Supervising personnel: Fill out monthly and return to Point of Care Testing Service by the end of the first
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How to fill out hemochron signature elite low

01
Turn on the Hemochron Signature Elite Low device.
02
Insert a clean, unused cuvette into the device.
03
Make sure the cuvette is properly loaded and the device is ready to use.
04
Collect a blood sample from the patient using a sterile needle and syringe.
05
Fill the cuvette with the blood sample according to the device's instructions.
06
Insert the cuvette into the device and follow the on-screen prompts to perform the test.
07
Wait for the results to be displayed on the screen.
08
Record the results and take necessary action based on the findings.

Who needs hemochron signature elite low?

01
Hemochron Signature Elite Low is typically used by healthcare professionals, particularly in clinical settings such as hospitals, laboratories, and medical offices.
02
It is commonly used for monitoring patients who require coagulation testing, such as those on anticoagulant therapy or undergoing surgical procedures.
03
Patients with bleeding disorders or clotting disorders may also benefit from tests performed with Hemochron Signature Elite Low.
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Hemochron Signature Elite Low is a specific type of blood coagulation testing device used to monitor patients on anticoagulant therapy, providing precise and rapid results.
Healthcare providers and laboratories that perform blood coagulation tests using the Hemochron Signature Elite device are required to file results and maintain compliance with regulatory standards.
To fill out the Hemochron Signature Elite Low, users should follow the manufacturer’s instructions, ensuring all patient information and test results are accurately recorded in the designated sections.
The purpose of Hemochron Signature Elite Low is to provide healthcare professionals with a means to assess a patient's coagulation status quickly, aiding in the management of patients on anticoagulant therapy.
The information that must be reported includes patient demographics, test type, test results, date and time of the test, and the healthcare provider's details.
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