Who is qualified to insert this device?

Insertion and removal should be performed by licensed clinicians trained in intrauterine device techniques. Facilities typically authorize gynecologists, family physicians, advanced practice providers, or trained clinicians per local policy. Teams should follow the manufacturer’s instructions and current professional guidance. Clinics often conduct periodic skills refreshers and maintain procedure checklists to support consistent technique and patient counseling across providers and sites.

What materials comprise the IUD?

The frame is medical‑grade polyethylene. Copper wire is wound around the stem and arms. No hormones are included. This configuration provides local contraceptive action through copper’s effect on sperm function within the uterus. Components are supplied sterile, single‑use, and intended for one patient encounter. Refer to the device label and the package insert for full specifications and any additional handling notes applicable to your facility.

Does the device include hormones or drugs?

No. This is a non‑hormonal, copper‑bearing intrauterine device. Copper’s local action reduces sperm viability and interferes with fertilization. Some patients may experience menstrual changes such as heavier bleeding, cramping, or spotting, especially in early cycles. Clinicians should assess medical eligibility, counsel on expected effects, and provide follow‑up consistent with current professional standards and the package insert.

What is included in the sterile pack?

Each unit arrives in a sealed, sterile pouch that contains the device and the insertion tools needed for placement. Labels show the product identifier, lot number, and expiration date to support traceability. The package is single‑use. Inspect the sterile barrier before use. Do not use if the pouch is damaged or opened. Dispose of used components according to your facility’s waste and sharps protocols.

How should unopened units be stored?

Keep pouches in a clean, dry area. Avoid crushing the box or compromising the sterile barrier. Store in the original packaging until the time of procedure. Confirm lot and expiry during intake and before placement. Facilities typically rotate stock using first‑to‑expire principles and document usage for traceability, aligning with internal device management policies.

What adverse effects are commonly reported?

Commonly reported effects include menstrual cramping, heavier or prolonged bleeding, and spotting, particularly in initial cycles. Some patients may experience discomfort during insertion or removal. Severe pain, fever, or unusual symptoms warrant evaluation. Clinicians should counsel on expected experiences, provide return precautions, and schedule follow‑up based on local protocols and the package insert. Report adverse events per institutional and regulatory requirements.

Can it be considered immediately postpartum?

Use timing is a clinical decision. Some programs include immediate postpartum insertion workflows within their protocols, while others prefer interval placement. Providers should consult current professional guidance, assess individual risk factors, and follow the manufacturer’s instructions. Ensure device availability, counseling materials, and post‑placement follow‑up processes are in place before scheduling immediate postpartum insertions.

T-Safe® CU 380A QL IUD

T-Safe® CU 380A QL IUD for Clinics

Name: Wholesale T-Safe® CU 380A QL IUD – Clinic Supply
SKU: 88876
Price: 334.99 USD
Availability: InStock

Intrauterine Device (Iud)

$334.99

Description

T‑Safe® CU 380A QL IUD is a small, T‑shaped intrauterine device designed for long-acting contraception in professional care. The system is placed intrauterinely by trained clinicians and supports programmatic family-planning services. For verified buyers, we provide US distribution to streamline procurement across sites and networks.

What T‑Safe Is and How It Works

This non‑hormonal device uses copper to create a local environment that reduces sperm viability and impedes fertilization. The CU 380A QL IUD features a plastic T‑frame with copper coiled around the stem and arms. Trained providers insert the product in a sterile setting following manufacturer instructions and applicable professional guidance.

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

The device is intended for long‑term contraception and may be removed whenever a patient and provider decide to discontinue use. Commonly observed effects can include cramping, heavier or prolonged bleeding, and spotting, especially in early cycles. Some individuals may report discomfort during insertion or removal. Clinicians should evaluate suitability and counsel on expected experiences according to current standards of care.

Professional Applications

Clinics integrate this product into family planning consults, routine gynecologic services, and community contraception programs. The system supports non‑hormonal pathways where predictable, device‑based contraception is preferred or requested. Teams may align scheduling for same‑day placement, interval insertion, or follow‑up visits based on internal protocols. In public health settings, it can complement counseling pathways and inventory strategies alongside other long‑acting options.

Programs may reference the intrauterine contraceptive device 380A QL within method counseling materials to distinguish non‑hormonal choices from progestin options such as the Nexplanon Implant or injectables like Depo-Provera. For workflow planning and stocking, see related categories: Contraceptives and Gynecology.

Key Features

Non‑hormonal copper mechanism: locally reduces sperm function.
T‑shaped, small‑profile frame for intrauterine placement.
Medical‑grade polymer construction suitable for clinical use.
Copper IUD 380A configuration with copper wound on stem and arms.
Single‑use, sterile packaging supports procedural efficiency.
Insertion tools included in the sterile pouch.
Designed for placement by trained healthcare professionals.
Clear labeling supports lot and expiry traceability.

Benefits in Practice

Non‑hormonal option: expands method mix during counseling.
Long‑acting format: reduces re‑supply visits once placed.
Workflow fit: standard IUD insertion techniques and tools.
Inventory control: single device per pouch simplifies counts.
Predictable handling: sterile, sealed presentation.
Program alignment: suitable for family planning initiatives.
Operational consistency: standard device class with known steps.
Patient education: clear talking points for expected effects.

Composition & Ingredients

The frame is medical‑grade polyethylene. Copper wire is wound around the stem and arms. No hormones are present. The copper contributes a local spermicidal effect that impairs sperm viability within the uterine cavity. This configuration supports long‑acting, reversible contraception under clinician supervision.

For catalog clarity and search, reference phrase alignment may include T-Safe copper IUD CU 380A QL as an identifier used by many clinical teams and procurement systems.

Packaging & Supply

Each unit is supplied sterile in a sealed pouch containing the device and the required insertion tools. The exterior label displays the product identifier, lot number, and expiry. Clinics should store unopened pouches in a clean, dry area per device best practices and avoid compromising the sterile barrier.

For inventory systems, note SKU 88876 when reconciling counts or building par levels. Each tsafe cu 380a ql unit is single‑use and intended for one patient encounter. Dispose of used or opened components according to your facility’s protocols for sharps and regulated waste.

Ordering & Logistics

Account verification is required. Sign in to view contract eligibility and submit purchase requests. Your team can align deliveries with clinic hours and consolidate shipments with other devices and supplies. If your formulary integrates multiple contraceptive options, consider adding this item to standing orders alongside related products in Medical Devices.

Order processing timelines depend on verification status and current availability. Confirm allocation needs early for multi‑site deployments. For any specific documentation requests or compliance notes, contact your account manager before finalizing the order.

Comparable Products

Clinics often evaluate similar copper devices or hormonal alternatives when configuring a method mix. For a copper T‑frame alternative with integrated loader, see Copper T 380A. For levonorgestrel‑releasing systems, review Levonorgestrel IUD and the smaller profile Low-Dose IUD. These options allow teams to tailor counseling and stocking strategies across patient needs and program goals.

Pricing & Access

Sign in to view available tiers for clinics and health systems. If your purchasing team tracks interest in T-Safe CU 380A QL IUD cost across budgets or grants, use your account to review current contract options. Volume structures may apply for eligible facilities, with quotes aligned to approval status and requested quantities.

Availability & Substitutions

Supply can vary by cycle and demand. Confirm current lead times before scheduling large insertion days or outreach events. If allocation is limited, your team may consider equivalent copper devices or appropriate hormonal alternatives after clinical review. When discussing substitutions for t safe cu 380a ql iud, verify compatibility with your protocols and provide staff refreshers for any device‑specific steps.

Authoritative Sources

Ready to add this item to your formulary? Sign in to confirm allocation and schedule shipments with temperature-controlled handling when required and tracked US delivery.

Frequently Asked Questions

Who is qualified to insert this device?
Insertion and removal should be performed by licensed clinicians trained in intrauterine device techniques. Facilities typically authorize gynecologists, family physicians, advanced practice providers, or trained clinicians per local policy. Teams should follow the manufacturer’s instructions and current professional guidance. Clinics often conduct periodic skills refreshers and maintain procedure checklists to support consistent technique and patient counseling across providers and sites.
What materials comprise the IUD?
The frame is medical‑grade polyethylene. Copper wire is wound around the stem and arms. No hormones are included. This configuration provides local contraceptive action through copper’s effect on sperm function within the uterus. Components are supplied sterile, single‑use, and intended for one patient encounter. Refer to the device label and the package insert for full specifications and any additional handling notes applicable to your facility.
Does the device include hormones or drugs?
No. This is a non‑hormonal, copper‑bearing intrauterine device. Copper’s local action reduces sperm viability and interferes with fertilization. Some patients may experience menstrual changes such as heavier bleeding, cramping, or spotting, especially in early cycles. Clinicians should assess medical eligibility, counsel on expected effects, and provide follow‑up consistent with current professional standards and the package insert.
What is included in the sterile pack?
Each unit arrives in a sealed, sterile pouch that contains the device and the insertion tools needed for placement. Labels show the product identifier, lot number, and expiration date to support traceability. The package is single‑use. Inspect the sterile barrier before use. Do not use if the pouch is damaged or opened. Dispose of used components according to your facility’s waste and sharps protocols.
How should unopened units be stored?
Keep pouches in a clean, dry area. Avoid crushing the box or compromising the sterile barrier. Store in the original packaging until the time of procedure. Confirm lot and expiry during intake and before placement. Facilities typically rotate stock using first‑to‑expire principles and document usage for traceability, aligning with internal device management policies.
What adverse effects are commonly reported?
Commonly reported effects include menstrual cramping, heavier or prolonged bleeding, and spotting, particularly in initial cycles. Some patients may experience discomfort during insertion or removal. Severe pain, fever, or unusual symptoms warrant evaluation. Clinicians should counsel on expected experiences, provide return precautions, and schedule follow‑up based on local protocols and the package insert. Report adverse events per institutional and regulatory requirements.
Can it be considered immediately postpartum?
Use timing is a clinical decision. Some programs include immediate postpartum insertion workflows within their protocols, while others prefer interval placement. Providers should consult current professional guidance, assess individual risk factors, and follow the manufacturer’s instructions. Ensure device availability, counseling materials, and post‑placement follow‑up processes are in place before scheduling immediate postpartum insertions.

Specifications

Main Ingredient: Copper
Manufacturer: Mona Lisa N.V.
Drug Class: Contraceptive Device
Generic Name: Copper T 380A
Package Contents: 38 OA 1IUD
Storage Requirements: Room Temperature (2℃~25℃)
Main Usage:

About the Brand

T-Safe

MedSafeHub, partnered with T-Safe, proudly brings premium yet affordable medical supplies within the reach of healthcare professionals and facilities. With T-Safe’s robust product line up, our platform medsafehub.com aims to prioritize patient safety and comfort by providing easy accessibility to our customers. Our association with T-Safe allows us to offer their top-notch products directly on our platform, MedSafeHub.com. This strategic collaboration not only simplifies the shopping process for healthcare providers but also saves them time and energy. They can effortlessly surf, select, and order their desired supplies from one dedicated platform. Furthermore, we offer competitive prices and assure dependable delivery, warranting that T-Safe products reach our customers swiftly and efficiently. A hallmark of high quality and effectiveness, T-Safe’s medical supplies inspire trust and reliability among its users. Upholding strict quality norms and employing state-of-the-art technologies, T-Safe ensures user-friendly and effective supplies. As such, by opting for T-Safe via MedSafeHub, healthcare providers can not only save valuable time but also ensure that their patients receive the highest standard of care.

Browse T-Safe Products

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

International Shipping

Seamless delivery across the world

Easy Returns

Flexible solutions with our 30 day return policy

Secure Payments

Order confidently with private security network