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SECTION A.1 SF 1449 SOLICITATION/CONTRACT/ORDER FOR COMMERCIAL ITEMS Table of Contents SECTION A 1 A.1 SF 1449 SOLICITATION/CONTRACT/ORDER FOR COMMERCIAL ITEMS 1 A.2 CONTRACT ADMINISTRATION DATA 3
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01
Start by placing the supine breast treatment device on a flat surface, such as a bed or examination table.
02
Ensure that the device is clean and sanitized before use.
03
Gently lift the patient's breasts and position them on the device, making sure they are comfortably supported.
04
Adjust the straps or fasteners on the device to secure it in place and ensure proper fit.
05
Verify that the patient is in a comfortable position and able to breathe easily.
06
If necessary, adjust the angle or position of the device to provide optimal treatment access.
07
Once the treatment is complete, assist the patient in removing the device while ensuring their comfort and modesty.
08
Clean and disinfect the supine breast treatment device according to the manufacturer's instructions before storing it for future use.

Who needs supine breast treatment device?

01
Patients undergoing supine breast treatment for various medical conditions or procedures.
02
Healthcare professionals who perform supine breast treatments, such as radiation therapists or oncologists.
03
Medical facilities and clinics that offer supine breast treatment services.
04
Individuals who prefer supine breast treatment as a non-invasive or alternative therapy.

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A supine breast treatment device is a medical equipment used for treating breast related issues while the patient is lying on their back.
Manufacturers or distributors of supine breast treatment devices are required to file for approval or registration.
The device should be filled out with accurate information regarding its specifications, usage, and any potential risks associated with its use.
The purpose of a supine breast treatment device is to provide effective treatment for breast conditions while ensuring patient comfort and safety.
Information such as device name, model number, intended use, components, and any warnings or precautions must be reported on the device.
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