What insertion training is recommended for this device?

Insertion should be performed by licensed clinicians trained in intrauterine device placement. Teams typically standardize a protocol that covers screening, aseptic technique, insertion steps, confirmation of position, and post-procedural monitoring. Many clinics use simulation or supervised initial cases to ensure consistent technique. Familiarity with ultrasound assessment and recognition of malposition signs can support quality and safety. Follow the manufacturer’s instructions for use and your institution’s clinical policies.

Who should not receive a copper IUD in clinic?

Clinical screening should rule out conditions that increase risk or reduce suitability. Contraindications include active pelvic infection, known uterine abnormalities that distort the cavity, pregnancy, and Wilson’s disease. Evaluate unexplained vaginal bleeding before insertion. Consider patient history of recent pelvic inflammatory disease and any anatomic or bleeding factors that may affect insertion or follow-up. Always follow accepted guidelines and local protocols when assessing eligibility.

How long does protection typically last with this device?

Copper intrauterine devices are used for sustained contraception and are recognized for long duration of action. Many programs reference up to ten years of use for this class, contingent on correct placement and clinical judgment. Actual duration should follow manufacturer guidance and local practice standards. Schedule routine follow-up to confirm positioning and review bleeding patterns. Removal and replacement can be scheduled when clinically indicated or when contraception needs change.

What side effects should patients be counseled about?

Common reactions after placement include cramping, spotting, irregular bleeding, and sometimes heavier or longer periods during the initial months. These effects often lessen over time. Counsel on when to seek care, such as severe pain, fever, unusual discharge, or inability to feel strings if previously palpable. Provide clear guidance on analgesia options and normal bleeding expectations. Document counseling and arrange follow-up based on your clinic’s protocol.

How is follow-up typically managed after insertion?

Most clinics schedule an early follow-up to assess symptoms, review bleeding, and confirm strings or position as indicated. Thereafter, periodic checks can be aligned with annual visits, or sooner if concerns arise. If malposition or expulsion is suspected, follow your protocol for imaging and management. Encourage patients to return for evaluation if they experience persistent pain, abnormal bleeding patterns, or signs of infection.

Can this copper IUD be used for nulliparous patients?

Many guidelines consider copper IUDs appropriate for nulliparous individuals after standard screening and counseling. The decision should reflect individual anatomy, tolerance for insertion, and informed preferences. Providers may use ultrasound or adjunct tools if insertion difficulty is anticipated. Discuss expectations around cramping and bleeding changes, and ensure access to timely follow-up if symptoms persist. Always align with current clinical guidance and your facility’s policies.

What should providers know about removal and reversibility?

Removal is performed by trained clinicians using the retrieval strings. Most removals are straightforward in the office setting. If resistance or missing strings occur, follow your protocol for evaluation and tools, and consider referral when indicated. The method is reversible, and fertility may return quickly after removal, though timing varies by individual. Provide counseling on alternative contraception or preconception planning as needed.

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SMB® TCu 380A with Safeload

SMB® TCu 380A with Safeload Intrauterine Device for Clinics

Name: Buy SMB® TCu 380A with Safeload – US Distribution
SKU: 89497
Price: 272.99 USD
Availability: InStock

Contraceptive Implant

$272.99

Description

This copper intrauterine device with a preloaded insertion system supports long-term, hormone-free contraception in clinical settings. It is stocked by clinics that offer reliable, reversible birth control placed in-office by trained clinicians. Inventory supports US distribution to licensed facilities.

What SMB Is and How It Works

SMB® TCu 380A with Safeload® is a copper-bearing intrauterine device intended for long-duration contraception under professional supervision. The device continuously releases copper ions inside the uterine cavity. These ions reduce sperm motility and viability in cervical and uterine fluids, which helps prevent fertilization. The Safeload mechanism supports controlled, consistent placement by trained providers using a sterile, single-use inserter.

This TCu 380A intrauterine device is hormone-free, reversible, and designed for sustained contraceptive protection. Typical reactions can include transient cramping, irregular bleeding, or heavier menses during early months after placement. It is not recommended for individuals with uterine abnormalities, active pelvic infections, or Wilson’s disease. Periodic follow-up helps confirm positioning and device function over time. Providers should follow accepted clinical protocols for insertion, confirmation, and removal.

Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.

Professional Applications

Clinics use this copper IUD in long-acting reversible contraception programs where hormone-free methods are requested. It fits well in structured contraception pathways that include counseling, point-of-care screening, and procedural placement. The product supports consistent workflows across gynecology services and family-planning visits.

The SMB TCu 380A IUD is suitable for practices that favor in-office device procedures with predictable steps. Teams can integrate it with intake forms, ultrasound confirmation where indicated, and routine post-placement checks. For additional contraceptive options and category breadth, review Contraceptives and Gynecology. For method counseling resources, see Nexplanon Implant, Depo-Provera Guide, and Ella Overview.

Key Features

Hormone-free option: Non-hormonal contraception with copper as the active component.
Long duration: Designed for extended protection when maintained in proper position.
Preloaded inserter: Sterile, single-use applicator to streamline placement steps.
Insertion control: Safeload design supports measured advancement and placement accuracy.
High compatibility: Fits clinic workflows for in-office device procedures.
Reversible method: Fertility generally returns after removal.
Known tolerability: Early cramping or irregular bleeding may occur and often settles.
Clinical screening: Not advised with uterine anomalies, active pelvic infection, or Wilson’s disease.
Follow-up readiness: Strings allow post-placement checks and removal when indicated.
Safeload copper IUD: Designed for precise and consistent insertion by trained providers.

Benefits in Practice

For clinical teams, this device supports standardized intake, placement, and follow-up without daily adherence requirements by the user. The hormone-free profile simplifies counseling when patients prefer non-hormonal methods or have reasons to avoid hormonal exposure. Preloaded delivery reduces preparation steps and can help decrease insertion variability across providers who follow the same protocol.

In inventory terms, a single sterile pack is straightforward to store, track, and prepare for scheduled procedures. The copper T 380A IUD form factor fits well into same-day contraception programs when screening criteria are met. Clinics can maintain continuity by pairing device placement with routine schedule blocks, allowing care teams to manage ultrasound, exam, and documentation within a single visit. Consistent device design helps reduce learning curve across new staff once the clinic’s protocol is established.

Follow-up steps are also predictable. Providers can confirm placement by exam or imaging where indicated and review bleeding expectations. Retrieval strings allow timely removal when transitioning methods or planning pregnancy. Overall, the product supports reliable, reproducible processes that are essential for quality and throughput in busy gynecology and family-planning services.

Composition & Ingredients

Active component: Copper, which releases ions locally in the uterine cavity.
Device structure: T-shaped frame designed for intrauterine placement by trained providers.
Retrieval element: Threads for identification of placement and removal by a clinician.
Inserter: Sterile, single-use applicator integrated with the device for procedural efficiency.

Packaging & Supply

The product is supplied as a sterile, single-use device preloaded in its insertion system to support efficient setup and placement. Packaging is intended to maintain sterility until the time of use. Clear labeling assists lot and expiry tracking for routine inventory management.

Each unit is designed for one procedure and should be handled using standard aseptic technique in line with clinic protocols. The SMB TCu 380A Safeload kit format helps reduce preparation variability, leaving fewer separate components to assemble. Storage is straightforward in normal clinic environments. Always check the label and integrity of the sterile barrier before use.

For broader device planning across service lines, your team can coordinate with materials management and reference the Medical Devices category for adjacent supplies.

Ordering & Logistics

Licensed buyers can sign in to confirm eligibility, view available configurations, and place orders under their facility account. Account verification ensures professional use by qualified providers. Contract and volume terms are available for high-utilization programs and multi-site systems. Please use SKU 89497 for accurate ordering and reconciliation.

After verification, your team can align order cycles with scheduled procedure blocks and maintain par levels to avoid appointment delays. Typical in-clinic handling requires only standard conditions; consult the manufacturer’s insert for any special storage conditions. For reference in counseling materials and service pages, many clinics describe this product as a copper IUD TCu 380A to emphasize the non-hormonal class.

Comparable Products

Clinics evaluating copper IUD options may also review T-Safe Cu 380A, which offers a similar class and form factor. For broader category context, you can explore Contraceptives and Gynecology. Teams comparing non-hormonal and hormonal pathways can reference Nexplanon Implant and Depo-Provera Guide for provider-facing education.

Pricing & Access

Sign in to view clinic pricing. Volume and contract tiers are available based on projected usage, purchasing cycle, and credentialed account status. Your representative can assist with formulary alignment, standing orders, and order consolidation for multi-site practices. Please reference SKU 89497 when discussing terms or setting replenishment schedules.

Availability & Substitutions

Supply may vary based on manufacturer production and distributor allocations. If a substitution is needed, confirm clinical equivalence and procedural fit with your care team before updating protocols. Alternate copper IUDs and selected hormonal LARC options may be available in our catalog; verify inserter compatibility, training requirements, and documentation updates prior to transition. We do not make restock guarantees, and lead times can change with market conditions.

Authoritative Sources

For clinical guidance on intrauterine contraception, refer to reputable, evidence-based resources:

Ready to streamline device supply for your contraception program? Sign in to order with temperature-controlled handling when required and tracked US delivery.

Frequently Asked Questions

What insertion training is recommended for this device?
Insertion should be performed by licensed clinicians trained in intrauterine device placement. Teams typically standardize a protocol that covers screening, aseptic technique, insertion steps, confirmation of position, and post-procedural monitoring. Many clinics use simulation or supervised initial cases to ensure consistent technique. Familiarity with ultrasound assessment and recognition of malposition signs can support quality and safety. Follow the manufacturer’s instructions for use and your institution’s clinical policies.
Who should not receive a copper IUD in clinic?
Clinical screening should rule out conditions that increase risk or reduce suitability. Contraindications include active pelvic infection, known uterine abnormalities that distort the cavity, pregnancy, and Wilson’s disease. Evaluate unexplained vaginal bleeding before insertion. Consider patient history of recent pelvic inflammatory disease and any anatomic or bleeding factors that may affect insertion or follow-up. Always follow accepted guidelines and local protocols when assessing eligibility.
How long does protection typically last with this device?
Copper intrauterine devices are used for sustained contraception and are recognized for long duration of action. Many programs reference up to ten years of use for this class, contingent on correct placement and clinical judgment. Actual duration should follow manufacturer guidance and local practice standards. Schedule routine follow-up to confirm positioning and review bleeding patterns. Removal and replacement can be scheduled when clinically indicated or when contraception needs change.
What side effects should patients be counseled about?
Common reactions after placement include cramping, spotting, irregular bleeding, and sometimes heavier or longer periods during the initial months. These effects often lessen over time. Counsel on when to seek care, such as severe pain, fever, unusual discharge, or inability to feel strings if previously palpable. Provide clear guidance on analgesia options and normal bleeding expectations. Document counseling and arrange follow-up based on your clinic’s protocol.
How is follow-up typically managed after insertion?
Most clinics schedule an early follow-up to assess symptoms, review bleeding, and confirm strings or position as indicated. Thereafter, periodic checks can be aligned with annual visits, or sooner if concerns arise. If malposition or expulsion is suspected, follow your protocol for imaging and management. Encourage patients to return for evaluation if they experience persistent pain, abnormal bleeding patterns, or signs of infection.
Can this copper IUD be used for nulliparous patients?
Many guidelines consider copper IUDs appropriate for nulliparous individuals after standard screening and counseling. The decision should reflect individual anatomy, tolerance for insertion, and informed preferences. Providers may use ultrasound or adjunct tools if insertion difficulty is anticipated. Discuss expectations around cramping and bleeding changes, and ensure access to timely follow-up if symptoms persist. Always align with current clinical guidance and your facility’s policies.
What should providers know about removal and reversibility?
Removal is performed by trained clinicians using the retrieval strings. Most removals are straightforward in the office setting. If resistance or missing strings occur, follow your protocol for evaluation and tools, and consider referral when indicated. The method is reversible, and fertility may return quickly after removal, though timing varies by individual. Provide counseling on alternative contraception or preconception planning as needed.

Specifications

Main Ingredient:
Manufacturer: SMB Corporation of India
Drug Class: Contraceptive
Generic Name: Intrauterine device (IUD
Package Contents: 1 IUD
Storage Requirements: Room Temperature (2℃~25℃)
Main Usage:

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