A Uterine Balloon Tamponade (UBT) is a specialized obstetric medical device designed to provide temporary mechanical control or reduction of postpartum uterine bleeding by applying pressure within the uterine cavity.
Also known as a PPH balloon tamponade, postpartum hemorrhage balloon, uterine tamponade catheter, obstetric hemorrhage balloon, Bakri-type balloon, or uterine balloon tamponade kit, the device is used by qualified healthcare professionals during selected cases of postpartum hemorrhage (PPH).
Postpartum hemorrhage is a serious obstetric emergency involving excessive bleeding following childbirth. One important cause is uterine atony, a condition in which the uterus does not contract adequately after delivery.
Uterine balloon tamponade works by creating mechanical pressure against the inner uterine walls. A purpose-designed balloon catheter is positioned by a trained clinician and filled with a manufacturer-approved sterile liquid. The resulting pressure may help reduce bleeding while the clinical team continues appropriate treatment and monitoring.
This is a temporary hemorrhage-control intervention, not a replacement for first-line treatment, blood transfusion, surgery, or comprehensive emergency obstetric care when required.
Depending on the manufacturer and model, a uterine tamponade device may feature:
A flexible balloon designed for uterine placement.
Medical-grade silicone or another manufacturer-approved material.
A catheter shaft.
A dedicated balloon-filling channel.
A compatible inflation port, valve, or stopcock.
A drainage channel on selected models.
Sterile, single-use construction.
Balloon capacity specified by the manufacturer.
Optional rapid-filling components.
Latex-free construction on selected products.
Individually sealed sterile packaging.
The uterine balloon tamponade price in Kenya depends on the brand, device design, balloon capacity, included accessories, packaging, manufacturer documentation, and institutional procurement quantity.
A reliable, currently advertised Kenyan retail price for an exact, manufacturer-identified uterine balloon tamponade device could not be independently established.
Historical international procurement literature provides the following indicative comparisons:
These figures originate from earlier research and health procurement assessments, rather than current Kenyan retail listings. They should not be used as today's selling prices, nor do they establish the cost of any particular Maesio product.
A hospital should request a current quotation specifying the exact device brand, model, sterility, capacity, package contents, and delivery requirements.
Device Type: A purpose-designed uterine balloon catheter and a low-cost tamponade kit are not equivalent products.
Manufacturer: Branded products may differ in material, documentation, design, and supplied components.
Balloon Capacity: Maximum permitted filling volumes vary between devices.
Drainage Channel: Some balloon catheters incorporate drainage to allow observation of ongoing uterine bleeding.
Rapid Filling Components: Additional tubing, valves, and bag spikes may be included with selected kits.
Material: Medical-grade silicone and other approved elastomers have different specifications.
Sterility: Devices for clinical use must meet their stated supply and sterility requirements.
Single-Use Packaging: Packaging quantity, shelf life, and sterile barrier integrity affect procurement.
Regulatory Documentation: Device traceability and applicable authorization documents should be verified.
Institutional Orders: Hospitals may request quotations based on their emergency obstetric equipment requirements.
Buy Uterine Balloon Tamponade in Kenya from Maesio Pharmaceuticals Limited for maternity hospitals, obstetric departments, emergency obstetric care facilities, and appropriately equipped referral hospitals.
Product: Uterine Balloon Tamponade – PPH Balloon Catheter or Kit
Category: Obstetric Equipment / Maternity Supplies / Postpartum Hemorrhage Management Devices
Device Type: Confirm whether a purpose-designed balloon catheter or a specified tamponade kit.
Material: Manufacturer-specific medical-grade material.
Balloon Capacity: Confirm exact maximum permitted capacity.
Drainage Channel: Present on selected models.
Sterility: Confirm sterile packaging.
Reusability: Purpose-designed postpartum balloon catheters are commonly single-use; confirm exact labeling.
Included Accessories: Confirm syringe, valves, tubing, and other components.
Clinical Application: Temporary control or reduction of selected postpartum uterine bleeding.
Delivery: Nairobi and countrywide Kenya, with East African delivery arrangements available by agreement.
Ordering Recommendation: Request an itemized quotation specifying the manufacturer, model, balloon capacity, sterile packaging, expiry date, and included accessories.
An exact Maesio product-specific URL could not be verified, so no unconfirmed product link has been included.
Healthcare facilities looking to buy uterine balloon tamponade in Nairobi should prioritize device identification, clinical suitability, sterility, and access to the other services needed for emergency postpartum hemorrhage management.
National referral hospitals.
County referral hospitals.
Private maternity hospitals.
Obstetric and gynecological departments.
Comprehensive emergency obstetric and newborn care facilities.
Obstetric operating theaters.
Specialist women's health hospitals.
Medical teaching and referral centers.
The presence of a UBT device alone does not establish that a facility is equipped to manage life-threatening postpartum hemorrhage.
A PPH balloon tamponade for sale in Kenya is intended to support selected clinical responses to postpartum hemorrhage.
The balloon provides internal pressure against the uterine wall.
Purpose-designed products use an appropriate flexible catheter and balloon material.
The balloon is filled using the method and liquid specified in the manufacturer's instructions.
Some devices include a separate drainage channel to help observe continued bleeding.
Commercial purpose-designed devices are commonly supplied sterile and intended for one patient.
The device forms part of a broader postpartum hemorrhage treatment protocol.
Devices may be supplied as individual catheters or kits containing specified accessories.
A postpartum hemorrhage balloon device in Kenya may be considered when bleeding due to uterine atony continues despite appropriate first-line treatment.
The World Health Organization's 2025 consolidated postpartum hemorrhage recommendations emphasize that uterine balloon tamponade should be used in settings where the following safeguards are available:
Standard first-line postpartum hemorrhage treatment.
Appropriate patient assessment and exclusion of other causes of bleeding.
Trained healthcare professionals.
Adequate monitoring.
Ready access to blood products.
Prompt surgical intervention when needed.
Uterine balloon tamponade must not delay escalation when bleeding remains uncontrolled.
Uterine Atony: Continued uterine bleeding associated with inadequate uterine contraction after childbirth.
Bleeding After Vaginal Delivery: The principal setting addressed by the WHO recommendation.
Bleeding Following Cesarean Delivery: Certain manufacturer-approved balloon devices may be used after cesarean birth, but clinical selection and the evidence base must be distinguished from the WHO recommendation for atony after vaginal birth.
Obstetric Emergency Management: UBT may be one component of specialist-led escalation where indicated.
A UBT device is not an appropriate universal treatment for every cause of postpartum bleeding. Trauma, retained placental tissue, uterine rupture, major arterial bleeding, and coagulation disorders require specific diagnosis and management.
Maesio Pharmaceuticals Limited supplies maternity equipment, obstetric instruments, medical consumables, diagnostic products, surgical equipment, and hospital supplies across Kenya and East Africa.
Hospitals seeking a uterine tamponade kit supplier in Kenya should confirm the complete device configuration and manufacturer instructions before purchasing.
Explore maternity and obstetric medical products through www.maesiopharmaceuticals.co.ke.
Manufacturer and brand.
Exact device model.
Purpose-designed balloon or tamponade kit.
Balloon material.
Maximum permitted filling capacity.
Catheter design and size.
Drainage lumen availability.
Syringe and valve compatibility.
Rapid-filling accessories.
Latex content.
Sterile packaging.
Single-use labeling.
Shelf life and expiry date.
Batch or lot traceability.
Storage requirements.
Applicable regulatory documentation.
Manufacturer instructions for use.
Institutional delivery requirements.
The Bakri is a purpose-designed silicone balloon catheter used for temporary control or reduction of postpartum uterine bleeding when conservative management is appropriate.
The manufacturer's documented maximum filling capacity is 500 mL.
Its catheter includes a drainage lumen, and some configurations are supplied with rapid instillation accessories.
Certain purpose-designed free-flow devices use balloon pressure while supporting observation of bleeding through a drainage pathway.
Their construction and allowable filling volumes depend on the specific manufacturer.
Some low-cost uterine tamponade systems use a catheter-and-balloon arrangement assembled or supplied as a kit.
The components, sterility, permitted use, and evidence base differ from those of a purpose-designed commercial device.
Such devices must not automatically be treated as equivalent to a Bakri balloon.
Selected commercial products incorporate compatible filling accessories.
A rapid instillation kit may include tubing, valves, and related accessories to support the device's approved filling process.
Different products may use alternative balloon shapes, catheter constructions, drainage systems, and maximum filling capacities.
Always refer to the exact device's instructions for use.
The following table describes the CooperSurgical Bakri Postpartum Balloon, a recognized example of a purpose-designed uterine tamponade device.
These specifications apply to the identified Bakri product only. They are not confirmed specifications for Maesio's unspecified uterine balloon tamponade listing.
The maximum inflation capacity is a safety limit, not an instruction to routinely fill the balloon to that volume.
The contents of a postpartum hemorrhage tamponade kit vary by manufacturer.
A purpose-designed balloon kit may include:
Additional obstetric supplies, medications, IV fluids, blood products, and surgical equipment are not automatically included.
The term uterine balloon tamponade does not establish that a device is an original Bakri product.
WHO notes that evidence is insufficient to determine the comparative effectiveness and safety of improvised versus purpose-designed devices.
Uterine packing uses suitable packing materials rather than a dedicated fluid-filled balloon to apply pressure or manage bleeding in selected circumstances.
A balloon catheter and uterine packing have different materials, placement considerations, monitoring requirements, and risks.
Neither should be substituted for the other without specialist clinical assessment.
Balloon tamponade relies on positive mechanical pressure within the uterine cavity.
Vacuum-induced uterine hemorrhage control devices use a different mechanism involving controlled negative pressure and uterine contraction.
Both require appropriate professional training, clinical assessment, and emergency obstetric infrastructure.
Temporary Mechanical Bleeding Control: May help reduce uterine bleeding in appropriately selected cases.
Additional Treatment Option: Can form part of a structured postpartum hemorrhage escalation pathway.
Purpose-Designed Construction: Commercial devices may offer defined balloon capacities, filling systems, and manufacturer documentation.
Drainage Monitoring Options: Certain models include drainage channels that support observation of ongoing blood loss.
Sterile Single-Use Availability: Designed products can be stocked for emergency obstetric use.
Maternity Equipment Preparedness: Appropriate availability may support institutional readiness when used alongside complete PPH treatment protocols.
These are intended functions and operational benefits. They do not guarantee successful hemorrhage control or avoidance of surgery.
Before purchasing:
Identify the required device category.
Confirm the manufacturer and product model.
Check the manufacturer's intended use.
Verify the maximum permitted balloon capacity.
Confirm the catheter and drainage configuration.
Review approved filling accessories.
Check material and latex specifications.
Verify sterile packaging and single-use labeling.
Confirm batch and expiry information.
Obtain the complete instructions for use.
Request applicable regulatory documentation.
Verify suitable storage conditions.
Confirm hospital training requirements.
Check compatibility with established PPH protocols.
Ensure surgical and transfusion backup arrangements.
Verify quantities needed for institutional stock.
Confirm stock availability and delivery arrangements.
Store the unopened device according to the manufacturer's stated temperature, humidity, and packaging requirements.
Before clinical use, qualified personnel should verify that the sterile packaging is intact and within its expiry date.
Purpose-designed devices such as the Bakri balloon are labeled single-use and must not be resterilized or reused.
Check for visible package damage, defects, missing components, or other issues identified in the manufacturer's instructions.
After use, the device and contaminated accessories must be disposed of according to the facility's clinical waste and infection-prevention procedures.
Hospitals should maintain appropriate stock rotation and document expiry dates for emergency obstetric products.
Postpartum hemorrhage is a medical emergency. Balloon tamponade should be performed only by appropriately trained healthcare professionals within a system capable of immediate escalation.
The following issues require careful clinical evaluation:
Continued heavy bleeding despite first-line treatment.
Retained placental tissue.
Genital tract trauma.
Suspected uterine rupture.
Coagulation disorders.
Signs of shock.
Need for blood transfusion or surgical intervention.
For the Bakri balloon specifically, manufacturer warnings include a maximum filling volume of 500 mL, use of sterile liquid rather than gas, and an indwelling duration not exceeding 24 hours.
These limits must not be transferred to other device brands without verification.
If bleeding persists or the patient's condition deteriorates, tamponade must not delay emergency treatment or surgery.
A reliable current retail price for an exact manufacturer-identified model could not be verified. Buyers should request a device-specific quotation.
You can inquire through Maesio Pharmaceuticals Limited for uterine tamponade devices and related maternity equipment.
It is a technique using a medical balloon device to provide temporary mechanical pressure inside the uterus to help reduce selected postpartum bleeding.
PPH stands for postpartum hemorrhage, meaning excessive bleeding after childbirth.
It is inadequate uterine contraction after delivery and is an important cause of postpartum hemorrhage.
Yes, for selected PPH due to uterine atony after vaginal birth when first-line treatment fails and specified safety conditions are met.
No. The cause of bleeding must be assessed and treated appropriately.
Not necessarily. Bakri is a specific branded uterine tamponade device.
CooperSurgical supplies the Bakri postpartum balloon product line.
The manufacturer's stated maximum inflation capacity is 500 mL.
No. Maximum permitted filling volume depends on the device.
No. It is the maximum for the named Bakri product, not a routine filling instruction.
The Bakri balloon must not be inflated with air or other gas. Follow the specific device's approved filling instructions.
Purpose-designed products such as the Bakri balloon are single-use.
Commercial purpose-designed products are commonly supplied sterile, but the selected packaging must be verified.
Some models, including the Bakri balloon, include a drainage lumen.
It provides a pathway for blood drainage that may assist the clinical team in monitoring ongoing bleeding.
The manufacturer's instructions describe use after vaginal or cesarean delivery. Clinical suitability must be assessed separately.
No. The WHO recommendation addresses selected cases that have not responded to standard first-line treatment.
No. Blood products and resuscitation may still be essential.
No. Surgical intervention may be urgently required if bleeding continues.
The manufacturer's maximum stated indwelling period is 24 hours.
No. Follow the exact manufacturer's instructions.
Only where the necessary staff, treatment protocols, monitoring, blood product access, and emergency surgical backup requirements are satisfied.
Yes. Correct patient selection, device use, monitoring, and emergency escalation require appropriate training.
They differ in design, materials, manufacturer documentation, and often drainage features.
Not automatically. WHO identifies important uncertainties in their comparative effectiveness and safety.
Yes, when the facility's approved emergency obstetric protocols include the specified device.
No. Kit contents are manufacturer dependent.
No. These are supplied in selected configurations.
Follow the manufacturer's packaging, temperature, humidity, and shelf-life instructions.
Products must be used according to their validated shelf life and manufacturer labeling.
Yes. Healthcare institutions may request quotations based on approved quantities and specifications.
No. It is an invasive emergency obstetric device for trained professionals.
Maesio Pharmaceuticals supplies medical products across Kenya and can arrange East African deliveries according to order requirements.
Confirm the device brand, model, balloon capacity, sterility, expiry date, drainage features, kit contents, regulatory documentation, and delivery arrangements.
Specification note: This table covers the uterine balloon tamponade product category. The Bakri specifications are provided only as a verified manufacturer example. The exact Maesio product's capacity, material, catheter design, included components, and permitted clinical use must be confirmed before publication.
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