What is the Medina (intrauterine device) IUD and how is it used for contraception?

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Last updated: December 8, 2025View editorial policy

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"Medina IUD" - Clarification Needed

There is no FDA-approved or recognized intrauterine device called the "Medina IUD" in current medical literature or contraceptive guidelines. This term does not appear in the U.S. Medical Eligibility Criteria for Contraceptive Use or standard contraceptive references 1.

Currently Available IUD Types

The established IUD categories recognized by the CDC include 1:

  • Copper-bearing IUD (Cu-IUD): Contains copper, provides contraception for up to 10 years 2
  • Levonorgestrel-releasing IUD (LNG-IUD): Releases 20 μg/24 hours of progestin, effective for 5 years 2, 3

Possible Explanations

You may be referring to:

  • Mirena IUD: A levonorgestrel-releasing device that is commonly used and may be phonetically confused with "Medina" 2
  • A regional or brand name: Some countries use different commercial names for standard IUD devices
  • A misspelling or miscommunication: The term may have been misheard or incorrectly transcribed

Standard IUD Contraceptive Mechanism

Both recognized IUD types work primarily by preventing fertilization rather than implantation 3. The copper IUD is immediately effective upon insertion and requires no backup contraception 4. The contraceptive efficacy is approximately 97%, with failure rates of 0.8% for copper IUDs and 0.1-0.2% for progestin IUDs in the first year 5.

Critical Safety Information

Absolute contraindications for any IUD include 1, 4:

  • Pregnancy (Category 4 - unacceptable health risk due to serious pelvic infection and septic spontaneous abortion risk)
  • Current pelvic inflammatory disease
  • Puerperal or post-septic abortion infection

Relative contraindications include 1, 4:

  • High risk for STIs at time of insertion (Category 3 for emergency contraception)
  • Unexplained vaginal bleeding 2

Recommendation for Clarification

Verify the exact name and type of IUD being referenced before proceeding with insertion or counseling, as using incorrect device information could lead to improper patient education or contraceptive failure.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Insertion and removal of intrauterine devices.

American family physician, 2005

Guideline

Copper T IUD Contraindications and Risks

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

The intrauterine device in modern contraception: Still an actuality?

The European journal of contraception & reproductive health care : the official journal of the European Society of Contraception, 2006

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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