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NOVAPLUS T 380 Ag NORMAL (Cu380+Ag) INTRAUTERINE DEVICE

NOVAPLUS T 380 Ag NORMAL (Cu380+Ag) INTRAUTERINE DEVICE

208٫00﷼السعر

NOVAPLUS T 380 Ag NORMAL (Cu380+Ag) INTRAUTERINE DEVICE
Product Description Technical features: 99,99% pure copper contraceptive wire + 0,1 mm Ø silver core380 mm2 of copper surface3 sizes available (maxi, normal and mini) that improve its fitting into the uterus ans increase the patient's comfortY-shaped IUDContraceptive safety up to 5 yearsPre-

loading insertion systemFor contraceptive purpose.

  • Section: Contraception
  • Sub Section: Contraceptive devices (View Prescribing Notes)
  • Drug Class: Intrauterine devices
  • Manufacturer: RF Medical Supplies

Novaplus T 380 Ag 

 Legal Class:

NC

 How Supplied:

Copper wire with silver core (surface area 380 mm2) on polyethylene stem with Y-shaped side arms and polyethylene thread.

 Price:

1 (normal or mini)=£12.50.

 Adults:

Replace after 5 years.

Novaplus T 380 Cu 

 Legal Class:

NC

 How Supplied:

Copper wire (surface area 380 mm2) on polyethylene stem with Y-shaped side arms and polyethylene thread.

 Price:

1 (normal or mini)=£10.95.

 Adults:

Replace after 5 years.

General warnings for Copper devices

 Contraindications:

Pregnancy, recent sexually transmitted infection, unexplained uterine or vaginal bleeding, distorted or small uterine cavity, genital malignancy, pelvic inflammatory disease, severe immunosuppression, Wilson's disease, medical diathermy, copper allergy.

 Warnings:

Should only be fitted by trained practitioners. History of ectopic pregnancy, previous tubal surgery, immunosuppression (avoid if severe), anaemia, menorrhagia, endometriosis, diabetes, nulliparity, young age, epilepsy, fertility problems, cervical disorders, increased risk of sexually transmitted infections. History of pelvic inflammatory disease. Valvular disease, history of endocarditis. Insertion before uterine involution complete—increased risk of expulsion. Insertion <36 weeks post-partum and/or breastfeeding—increased risk of uterine perforation. Examine 3—6 weeks after insertion, then annually. If threads not visible, exclude pregnancy; if excluded and threads cannot be found, consider possibility of expulsion or perforation.

 Interactions:

Anticoagulants.

 Adverse Effects:

Uterine/cervical perforation, pelvic infection, abnormal bleeding, allergic reaction. On insertion: Pain, bleeding; rarely, epileptic seizure, vasovagal attack.
REASONS FOR REMOVAL: Excessive or persistent bleeding or cramping. Perforation of uterus or cervix. Displacement from uterine cavity. Refractory pelvic infection. Pregnancy.

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