What is included with the device packaging?

Each unit arrives as a single sterile, single-use IUD in a sealed pouch, ready for insertion with standard technique. The outer packaging displays the lot number and expiration to support inventory control and documentation. No inserter accessories beyond the supplied delivery system are included. Inspect the sterile barrier before opening. If the pouch is damaged or opened, follow your facility policy for quarantine and replacement and do not use the device for insertion.

How long can this system remain in place?

The system is intended for long-acting use and provides up to three years of contraceptive coverage when placed and maintained according to clinical guidance. Removal or exchange can occur at any time if plans change or if clinical considerations require it. Establish recall reminders within your EHR to support timely follow-up and device replacement scheduling. Always evaluate individual factors during counseling and confirm the recommended duration against current guidelines.

What adverse events should our team counsel about?

Counsel that irregular bleeding patterns are common in the first months after insertion. Other reported effects include headache, abdominal pain, nausea, and breast tenderness. Serious but uncommon events include expulsion, uterine perforation, and pelvic inflammatory disease. Provide instructions for recognizing warning symptoms and when to seek evaluation. Encourage follow-up to check strings and position per your protocol, and consider imaging if expulsion or malposition is suspected after insertion.

How does this compare with copper IUDs or higher-load systems?

This device releases levonorgestrel locally, whereas copper IUDs are hormone-free. Compared with higher-load systems, it may be selected for those preferring a lower total hormone content and three-year duration. Selection should balance desired duration, frame size, insertion familiarity, and clinic inventory strategy. Review comparable options such as copper devices or higher-load levonorgestrel systems, and align the choice with your service model and counseling approach.

Are there specific storage or handling requirements?

Follow the manufacturer’s labeled storage conditions and your facility procedures. Keep the unit in its sealed sterile pouch until the time of insertion. Avoid exposure to conditions that might compromise packaging integrity. Do not resterilize. Dispose of used components per your sharps and medical device handling policies. If you maintain decentralized stock, rotate inventory so that earlier expiry lots are used first and reconcile counts during monthly checks.

Can this be used immediately after delivery or abortion?

Timing of insertion should follow current clinical guidelines and individual assessment. Immediate or delayed placement may be considered based on uterine size, involution, and infection risk, as determined by the clinician. Ensure informed counseling about expulsion risk and follow-up. For postpartum or postabortion workflows, standardize protocols for eligibility screening, insertion timing, and string management, and document decisions within your facility’s pathway.

What training does staff need for safe placement?

Placement should be performed by clinicians trained in intrauterine device insertion and removal. Establish competency validation, supervision for new inserters, and access to troubleshooting support. Maintain availability of appropriate instruments, analgesia options per protocol, and ultrasound or pelvic exam resources when needed. Post-insertion care instructions and return precautions should be standardized across providers to ensure consistent counseling and follow-up scheduling.

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Jaydess®

Jaydess® 13.5 mg IUD for Clinics

Name: Wholesale Jaydess® IUD – Clinic Supply
SKU: 88862
Price: 402.99 USD
Availability: InStock

Hormonal Contraceptive

$402.99

Description

This small, T-shaped intrauterine device is designed for office-based contraception. The system releases a progestin locally within the uterus and supports long-acting, reversible use for appropriate candidates. Clinics keep this class on hand to streamline insertion days, standardize workflows, and offer multi-year coverage within family planning services. Our US distribution enables dependable replenishment aligned to your schedule.

What Jaydess Is and How It Works

The Jaydess® levonorgestrel IUD is a hormone-releasing intrauterine system placed by a trained clinician during a brief in-office procedure. Once positioned, the device releases a low daily amount of levonorgestrel directly into the uterine cavity. This local delivery supports contraceptive protocols by thickening cervical mucus and creating an endometrial environment that is not conducive to fertilization. It is a long-acting reversible option and can be removed at any time if plans change. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.

This preparation is supplied sterile for single use and is intended for insertion using standard IUD techniques. It may be integrated into routine gynecology visits or scheduled LARC sessions. Training and competency validation remain at the discretion of the medical director.

Professional Applications

Clinics use this system in reproductive health programs, primary care women’s services, and multidisciplinary practices offering long-acting contraception. It fits appointment blocks for new starts, exchanges, and removals with predictable chair time. The Levonorgestrel 13.5 mg IUD also supports service-line continuity when counseling individuals who prefer a low-dose, intrauterine option. Practices may incorporate it alongside implants and injectables as part of comprehensive contraceptive counseling.

For program development and cross-training resources, see category collections such as Contraceptives and Gynecology, and review related reads like Nexplanon Implant, Depo-Provera Guide, and Ella Emergency Pill.

Key Features

Long-acting option: supports up to three years of contraceptive use in suitable candidates.
Local hormone delivery: levonorgestrel released within the uterus for targeted effect.
Small T-shaped frame: designed for straightforward placement with standard technique.
Sterile single-use unit: supplied ready for insertion in a sealed pouch.
Clinic-focused workflow: predictable chair time and streamlined follow-up scheduling.
Jaydess® device: brand-name product from a major manufacturer.
Adverse event profile: common effects may include irregular bleeding, headache, abdominal pain, nausea, or breast tenderness.
Serious risks, rare: expulsion, uterine perforation, and pelvic inflammatory disease can occur; evaluate and counsel per protocol.

Benefits in Practice

This class integrates well into routine gynecologic schedules. The device is single-use, sterile, and ready for insertion, which supports quick room turnover. Inventory is simple to track, and the compact package helps conserve cabinet space. Training pathways are familiar for teams already placing IUDs.

The Jaydess® birth control IUD can help align counseling and placement in a single visit, reducing return appointments when clinically appropriate. Standardized device selection also simplifies procurement and minimizes variation in supply across providers and satellite locations. The predictable three-year service life supports recall lists and electronic reminders for exchange or removal.

Because the system is removable at any time, it supports shared decision-making over the full use period. Clinics can manage removals and exchanges with brief appointments, limited instrumentation, and consistent room setup.

Composition & Ingredients

Active ingredient: levonorgestrel, total content 13.5 mg.
Device platform: T-shaped intrauterine system designed for local hormone release.

No additional excipient details are provided here. Refer to the enclosed manufacturer literature for full component information and material disclosures.

Packaging & Supply

This product is supplied as a single IUD packaged in a sterile pouch for one-time use. The total levonorgestrel content of 13.5 mg is stated on the label, with lot number and expiry clearly printed to support traceability. Units are individually pouched to assist controlled dispensing from central supply or clinic rooms. Store and handle per the manufacturer’s labeling. SKU: 88862.

Each pouch arrives sealed; do not use if the sterile barrier is compromised. Dispose of all components per your facility’s sharps and device policies after use.

Ordering & Logistics

Account verification is required for purchasing. Sign in to view contract tiers and current availability. Your team can place orders through our portal, designate primary and backup shipping addresses, and assign buyer permissions for multi-site practices. Lead times vary by location and order volume; your dashboard provides current estimates and order confirmations.

For formulary alignment, we can map this item to internal codes and assist with substitution rules when cross-referencing comparable devices. Contact your representative if you require standing orders for scheduled insertion days or centralized inventory routing.

Comparable Products

Clinics often evaluate within-class alternatives to fit patient profiles and service-line preferences. Consider a higher-load system such as Mirena IUD, or a hormone-free option like T-Safe Cu 380A. Selection should be guided by clinical protocols, insertion experience, and follow-up workflows.

Pricing & Access

Sign in to view pricing. Volume and contract tiers are available for qualified facilities, including multi-site organizations and training programs. Your account manager can assist with quotations for scheduled procurement cycles and consolidated billing.

Availability & Substitutions

Supply can vary based on manufacturer production and regional demand. If this item is temporarily unavailable, we can suggest suitable substitutions within your approved formulary, subject to medical director review. Confirm any substitution against your clinical guidance and documentation requirements before updating orders.

Authoritative Sources

For detailed prescribing and device information, consult manufacturer and regulatory resources:

Ready to proceed? Verify your account, add to cart, and schedule fulfillment with temperature-controlled handling when required and tracked US delivery.

Frequently Asked Questions

What is included with the device packaging?
Each unit arrives as a single sterile, single-use IUD in a sealed pouch, ready for insertion with standard technique. The outer packaging displays the lot number and expiration to support inventory control and documentation. No inserter accessories beyond the supplied delivery system are included. Inspect the sterile barrier before opening. If the pouch is damaged or opened, follow your facility policy for quarantine and replacement and do not use the device for insertion.
How long can this system remain in place?
The system is intended for long-acting use and provides up to three years of contraceptive coverage when placed and maintained according to clinical guidance. Removal or exchange can occur at any time if plans change or if clinical considerations require it. Establish recall reminders within your EHR to support timely follow-up and device replacement scheduling. Always evaluate individual factors during counseling and confirm the recommended duration against current guidelines.
What adverse events should our team counsel about?
Counsel that irregular bleeding patterns are common in the first months after insertion. Other reported effects include headache, abdominal pain, nausea, and breast tenderness. Serious but uncommon events include expulsion, uterine perforation, and pelvic inflammatory disease. Provide instructions for recognizing warning symptoms and when to seek evaluation. Encourage follow-up to check strings and position per your protocol, and consider imaging if expulsion or malposition is suspected after insertion.
How does this compare with copper IUDs or higher-load systems?
This device releases levonorgestrel locally, whereas copper IUDs are hormone-free. Compared with higher-load systems, it may be selected for those preferring a lower total hormone content and three-year duration. Selection should balance desired duration, frame size, insertion familiarity, and clinic inventory strategy. Review comparable options such as copper devices or higher-load levonorgestrel systems, and align the choice with your service model and counseling approach.
Are there specific storage or handling requirements?
Follow the manufacturer’s labeled storage conditions and your facility procedures. Keep the unit in its sealed sterile pouch until the time of insertion. Avoid exposure to conditions that might compromise packaging integrity. Do not resterilize. Dispose of used components per your sharps and medical device handling policies. If you maintain decentralized stock, rotate inventory so that earlier expiry lots are used first and reconcile counts during monthly checks.
Can this be used immediately after delivery or abortion?
Timing of insertion should follow current clinical guidelines and individual assessment. Immediate or delayed placement may be considered based on uterine size, involution, and infection risk, as determined by the clinician. Ensure informed counseling about expulsion risk and follow-up. For postpartum or postabortion workflows, standardize protocols for eligibility screening, insertion timing, and string management, and document decisions within your facility’s pathway.
What training does staff need for safe placement?
Placement should be performed by clinicians trained in intrauterine device insertion and removal. Establish competency validation, supervision for new inserters, and access to troubleshooting support. Maintain availability of appropriate instruments, analgesia options per protocol, and ultrasound or pelvic exam resources when needed. Post-insertion care instructions and return precautions should be standardized across providers to ensure consistent counseling and follow-up scheduling.

Specifications

Main Ingredient: Levonorgestrel
Manufacturer: Bayer Healthcare Pharmaceuticals Inc.
Drug Class: Hormonal Contraceptive
Generic Name: Levonorgestrel-Releasing Intrauterine System
Package Contents: 13.5 mG 1UD
Storage Requirements: Room Temperature (2℃~25℃)
Main Usage:

About the Brand

Jaydess

Renowned as a top-notch healthcare brand, Jaydess furnishes trustworthy and potent birth control solutions for women around the globe. The brand specializes in intrauterine devices (IUDs), gifting women with a hassle-free and enduring contraceptive alternative. A distinctive perk of Jaydess is its availability on our online storefront, medwholesalesupplies.com, enabling healthcare units and clinicians to fetch this product in substantial quantities, hence assuring a dependable and efficient birth control solution to patients. Medwholesalesupplies.com comprehends the significance of unimpeded and credible access to medical provisions for health professionals. This understanding drives us to render Jaydess, and other premium products on our online store. Procuring Jaydess via medwholesalesupplies.com lets medical practitioners economize their time and energy by buying straight from a reputable source. Moreover, our store presents cost-effective deals and accelerated delivery choices, enabling health institutions to replenish their stock promptly and address their patient's requirements. Jaydess is an IUD offering extended birth control for a span of three years. With an extremely low failure rate of under 1%, it stands as a highly effective measure. Through our portal, medwholesalesupplies.com, we ensure health practitioners gain access to this reliable and well-founded contraceptive choice. By buying Jaydess in large quantities from our online store, health professionals can keep this birth control alternative handy, thereby improving their patient care services by offering a dependable and efficient contraceptive method.

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