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ADA247 385 III I llIIiIlIIItlll IL TECHNICAL REPORTjAD9116INtRAVENOUS (IV) FLUIDIZER IV. A DISPOSABLE DEVICE FOR PREPARATION OF STERILE WATER FOR INJECTION IN A FIELD SETTING. DICKINSON BURROWS, PhD,
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01
Start by gathering all the necessary equipment: sterile water, sterile container, gloves, mask, and sterile syringe.
02
Wash your hands thoroughly with soap and water before beginning the process.
03
Put on gloves and a mask to prevent contamination.
04
Open the sterile water container carefully to avoid any contamination.
05
Use a sterile syringe to draw up the appropriate amount of sterile water.
06
Carefully transfer the sterile water into the sterile container, making sure to avoid touching anything non-sterile.
07
Close the sterile container tightly to prevent any contamination.
08
Label the sterile water container with the date and time it was created.
09
Store the sterile water in a clean and dry place, away from direct sunlight or heat.
10
Use the sterile water as needed, and discard any unused portion after the expiration date.

Who needs creating sterile water for?

01
Sterile water is needed for medical procedures such as wound cleaning, intravenous medication administration, and medical device sterilization.
02
It is also used in laboratories for preparing agar plates, diluting samples, and other scientific experiments.
03
Pharmaceutical companies may require sterile water for drug formulation and manufacturing processes.
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Creating sterile water is primarily for use in medical applications, including dissolving medications for injection or as a diluent in laboratory procedures.
Manufacturers and facilities that produce sterile water for medical use are required to file documentation to comply with regulatory standards.
The process involves adhering to specific protocols for aseptic technique, ensuring proper labeling, and maintaining records of production to ensure compliance with regulatory guidelines.
The purpose is to provide a contamination-free solution that can be used safely in medical treatments, surgeries, and laboratory tests.
Information that must be reported includes batch numbers, production dates, expiration dates, and compliance with safety and quality standards.
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