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Get the free Jaydess Sistema intrauterino 13.5 mg - ISP

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Ref.: RF366098/12Reg.ISP N: F19985/13 FILLET DE Information AL PROFESSIONAL JADES SYSTEM INTRAUTERINE 13.5 mg Institute DE Salad Buck DE CHILE STI NATIONAL DE IlEDlCAMENTOS OFFICIAL PRODU1.NOMBREDEL
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01
Wash your hands thoroughly before handling the Jaydess intrauterine system (IUS).
02
Find a comfortable position, such as lying down with your knees bent, for insertion.
03
Open the Jaydess package and remove the applicator from the sterile packaging.
04
Hold the applicator firmly and insert the IUS into the applicator until the end of the threads is visible.
05
Rest the Jaydess applicator on the opening of your vagina and gently push it upwards until it reaches the top of your uterus.
06
Release the IUS by pushing the plunger until it stops.
07
Slowly pull the applicator out, ensuring that the IUS remains in place.
08
Check that the threads are hanging down from your cervix, as this indicates proper placement.
09
After insertion, wash your hands again and discard the applicator in a proper disposal container.
10
Follow up with your healthcare provider to ensure proper placement and to discuss any concerns or side effects.

Who needs jaydess sistema intrauterino 135?

01
Jaydess sistema intrauterino 135 is a contraceptive device that is suitable for women who want long-term birth control.
02
It is specifically designed for women who have not had children or who have had only one child.
03
Women who prefer a hormone-based contraceptive method that provides up to 3 years of protection may consider Jaydess IUS 135.
04
It is important to consult with a healthcare provider to determine if Jaydess IUS 135 is the right contraceptive option for you.
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It is a type of intrauterine system for contraception.
Healthcare professionals who prescribe or insert the device are required to file the form.
The form must be completed with relevant patient information and details of the insertion procedure.
The purpose is to track the use of the contraceptive device and monitor any potential side effects or complications.
Patient demographics, insertion details, follow-up information, and any adverse events must be reported.
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