Mirena® IUD for Clinics
$397.99
Description
What Mirena Is and How It Works
Mirena® is a small, T-shaped intrauterine device placed by a trained clinician for long-acting reversible contraception. It releases levonorgestrel locally within the uterus after placement. Clinics maintain inventory for insertion visits and postpartum programs, with US distribution supporting efficient restocking.
Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors. This hormonal intrauterine system functions by steadily releasing progestin from a polymer core. It is intended for professional use under sterile technique and appropriate clinical assessment. Many clinics specify Mirena English to align documentation, billing, and charting with English-language packaging and instructions.
Professional Applications
This IUD integrates into gynecologic services focused on long-acting contraception. It suits outpatient procedural rooms and postnatal services where device placement can be completed during scheduled visits. Teams often standardize lot tracking and follow-up scheduling within electronic records to coordinate device checks and removals.
Clinicians may include the Mirena contraceptive IUD in counseling pathways alongside other reversible methods. Practices commonly list this option within their Contraceptives and Gynecology protocols so staff can reference device availability and procedural steps. Inventory leads may also coordinate equipment through Medical Devices categories and related training resources. Some teams compare this IUD to the implant pathway; see our brief clinical article on the Implant Option for context.
Key Features
- T-shaped device: compact frame designed for intrauterine placement.
- Localized hormone release: supports long-acting, reversible contraception.
- Clinician-inserted: placement and removal by trained healthcare professionals.
- Single sterile unit: each unit arrives ready for aseptic insertion workflow.
- Flexible arms and tail threads: designed to aid centering and later retrieval.
- Clear IFU inclusion: carton includes instructions for use in English.
- Mirena English packaging: supports documentation needs and staff training.
- Sealed system: sterile barrier maintained until opened at the point of care.
Benefits in Practice
Long-acting devices fit clinic schedules well. A brief procedure can support months to years of contraceptive coverage with a single placement. This product helps consolidate inventory management to fewer, predictable reorder points. Standardized lot and expiry capture also simplifies compliance with internal protocols.
Teams value consistent handling requirements and compact storage. Setup needs remain modest and compatible with most outpatient procedure rooms. Mirena in English also streamlines patient communications, discharge notes, and interdepartmental coordination when multiple teams share responsibility for follow-up.
For administrative workflows, a single sterile presentation reduces picking errors. Packaging is straightforward and easy to stage on procedure carts. Supply teams can align device allocation with appointment volumes, reducing last-minute scrambles and overflow stock.
Composition & Ingredients
The device contains a synthetic progestin reservoir that releases levonorgestrel gradually into the uterine cavity. It is built on a soft, flexible polymer frame and includes retrieval threads designed for visual confirmation and removal. As a category description, a Levonorgestrel-releasing IUD 52 mg is widely recognized among clinicians; confirm device specifics against the carton and IFU at intake.
Adverse reactions may occur. Commonly reported events include irregular bleeding or spotting, changes in menstrual patterns, headache, nausea, and breast tenderness. Serious but infrequent events have been reported, including infection, uterine perforation, and ectopic pregnancy. Evaluate risks, contraindications, and patient suitability prior to placement, and align with clinic protocols for post-insertion monitoring.
Packaging & Supply
This line ships as a single, sterile device sealed within protective packaging. The carton includes an English-language insert for professional reference. Labels present essential identifiers for intake and documentation, including lot and expiry, supporting accurate EHR entry and device tracking policies. Confirm sterilization dating and package integrity upon receipt and prior to use.
For clinics aligning stock by active and strength notation, the package reflects the class and strength used in professional references, such as Mirena levonorgestrel 52 mg IUD. Maintain first-expire-first-out practices. Store in a secure area dedicated to procedure inventory to avoid cross-mixing with non-procedural supplies. Do not use if the seal is broken or the sterile barrier appears compromised.
Ordering & Logistics
Access is limited to licensed healthcare entities. Create or verify your account to view allocation options and request quotes. After account verification, sign in to review volume tiers and contract opportunities. Our team coordinates fulfillment through vetted distributors, with dispatch windows dependent on allocation and warehouse position. Your operations team can specify carton language needs during the request stage when appropriate.
Provide a receiving contact and hours to avoid delays. On arrival, record lot and expiry in your system before moving stock into secure storage. Please follow your clinic’s device governance for chain-of-custody and peri-procedure handling.
Comparable Products
Clinics often consider a smaller hormonal IUD when patient selection favors reduced dimensions; see Jaydess IUD for a lower-dose alternative. If a non-hormonal option is required, copper devices such as Copper IUD 380A and the TCu 380A Option provide hormone-free contraception. These options can be listed alongside this preparation to support shared decision-making pathways and inventory flexibility.
For broader planning, review related categories and maintain an updated formulary across methods. The mix across hormonal and non-hormonal devices can reduce scheduling bottlenecks.
Pricing & Access
Sign in to view pricing for your verified clinic account. Volume and contract pricing may be available based on order cadence and allocation size. Multi-site organizations can request consolidated quotes to align budgets across locations. Formal quotes typically reference lot windows expected at the time of allocation, so verify timing if your clinic requires synchronized restocking across sites.
Availability & Substitutions
Supply can vary based on distributor allocation and regional demand. If this item is temporarily constrained, your account manager can discuss suitable alternatives from the same class or non-hormonal lines. Confirm interchangeability and procedural impacts within your clinical governance before substituting any device.
We recommend maintaining a modest buffer of approved alternatives to avoid rescheduling procedures. Record any substitution decisions in your formulary and update staff checklists accordingly.
Authoritative Sources
Ready to allocate inventory for upcoming procedures? Sign in to request supply with temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
How does this hormonal IUD fit into clinic workflows?
This device suits outpatient gynecology services and postpartum programs where a brief procedure provides long-acting contraception. Teams typically prepare a small sterile setup, validate patient eligibility, and capture lot and expiry in the EHR. Scheduling includes a device check or follow-up per clinic protocol. Some practices maintain copper IUDs and an etonogestrel implant as alternatives, so counselors can match method preferences while keeping procedure rooms moving efficiently.
What storage and handling considerations apply before placement?
Store the sterile unit in a clean, secure location away from environmental stressors. Inspect the outer wrap for damage and confirm the seal remains intact before bringing it to a procedure room. Verify lot and expiry on intake. Do not open the sterile barrier until setup begins under aseptic technique. If the package is compromised or labeling is unclear, quarantine the unit and follow your clinic’s device governance before use.
What is included in the packaging for clinical use?
Each carton typically contains one sterile device sealed in protective packaging and an English-language instructions-for-use leaflet. Labels present identifiers suitable for EHR capture, including lot and expiry. The simple presentation supports quick setup on procedure carts. If your site requires language-specific materials for documentation or training, verify the carton language at the time of allocation and on receipt.
What side effects should teams discuss during counseling?
Counseling often includes irregular bleeding or spotting, menstrual changes, headache, nausea, and breast tenderness as commonly reported events. Serious but infrequent events may include infection, uterine perforation, and ectopic pregnancy. Discuss contraindications and consider individual risk factors before placement. Ensure patients know how to access care if they experience pelvic pain, fever, or symptoms suggestive of pregnancy after insertion.
Who should perform insertion and removal?
A trained healthcare professional should perform insertion and removal under sterile technique. Many clinics credential clinicians through internal competency programs and maintain checklists for equipment, timeout, and post-insertion counseling. If your team is building capacity, consider simulation training and precepted procedures. Always follow the instructions for use and your clinic’s procedural policies to support consistent outcomes and safety.
How can we streamline documentation and device tracking?
Standardize intake and procedure checklists that include lot, expiry, carton language, and operator identifiers. Capture device details in the EHR at receipt and at insertion. Some sites affix removable lot stickers to the consent or procedure note. Align storage locations with barcode scanning to reduce picking errors. Routine reconciliation during cycle counts helps ensure procedural rooms are stocked with the intended devices.
What alternatives should we keep on hand if allocation is constrained?
Maintain at least one copper IUD and, if appropriate, a smaller hormonal IUD. Consider stocking a limited number of implants for patients who prefer a non-uterine method. For example, a copper 380A device and a lower-dose hormonal device can cover most counseling scenarios. Review your formulary, procurement cadence, and staff training to decide which alternatives best support clinic throughput and patient-centered choices.
Specifications
- Main Ingredient: Levonorgestrel
- Manufacturer: Bayer Pharmaceuticals
- Drug Class: Contraceptive
- Generic Name: Levonorgestrel-Releasing Intrauterine System
- Package Contents: 52 mg - 1 IUD
- Storage Requirements: Room Temperature (2℃~25℃)
- Main Usage:
About the Brand
Mirena
Here to help
Questions about ordering, delivery or products? You can email our team here or call now at 1-800-630-9757 and be connected with your dedicated Account Manager
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