The Diacap Pro19H Dialyzer is a sterile, single-use, high-flux hollow-fibre haemodialysis dialyzer manufactured by B. Braun for professional renal replacement therapy.
Also known as the B. Braun Diacap Pro 19H, Diacap 1.9m² High-Flux Dialyzer, B. Braun Polysulfone Dialyzer, Diacap Pro19H Haemodialysis Filter or High-Flux Artificial Kidney Filter, this product is designed to support the removal of selected waste substances and excess fluid from the blood during prescribed haemodialysis treatment.
Haemodialysis is a medical treatment used for patients whose kidneys cannot adequately remove certain waste products, regulate fluid balance or maintain appropriate electrolyte levels.
During treatment, blood circulates through an extracorporeal circuit and passes through a dialyzer containing a semipermeable membrane.
The membrane separates the blood from the dialysis fluid while allowing appropriate transport of water and dissolved substances according to their characteristics and the prescribed treatment conditions.
The Diacap Pro19H belongs to B. Braun's Diacap Pro high-flux dialyzer range.
It features a 1.9m² polysulfone membrane surface area, providing a defined filtration surface for appropriate haemodialysis treatment.
The membrane is arranged in a hollow-fibre configuration within a polycarbonate housing.
This construction provides separate blood and dialysate pathways, allowing controlled exchange across the semipermeable membrane.
The product has a manufacturer-specified blood-side priming volume of 120mL.
Priming volume is an important characteristic of the extracorporeal circuit and should be considered when selecting a dialyzer for the patient's clinical requirements.
The Diacap Pro19H is a high-flux dialyzer, meaning that its membrane is designed for relatively high water permeability compared with conventional low-flux membranes.
High-flux dialysis may support clearance of selected larger solutes when used under suitable treatment conditions.
However, actual solute clearance and fluid removal depend on the dialysis prescription, machine performance, blood flow, dialysate flow, treatment duration and patient characteristics.
B. Braun identifies the 720DH19G model as a sterile, disposable high-flux dialyzer.
The membrane material is polysulfone, while the housing is made from polycarbonate.
The manufacturer confirms that the product does not contain latex or DEHP.
The dialyzer is supplied sterile following gamma sterilization and is intended for one patient and one treatment.
The Diacap Pro19H Dialyzer is suitable for appropriately equipped hospitals, dialysis centres and renal care facilities providing prescribed haemodialysis treatment.
It must be used only by trained healthcare professionals with compatible haemodialysis equipment and an appropriate extracorporeal blood circuit.
Manufacturer: B. Braun.
Product Family: Diacap Pro.
Model: Pro19H.
Manufacturer Reference: 720DH19G.
Product Type: High-Flux Haemodialysis Dialyzer.
Membrane Technology: Hollow-fibre membrane.
Membrane Surface Area: 1.9m².
Membrane Material: Polysulfone.
Housing Material: Polycarbonate (PC).
Blood-Side Priming Volume: 120mL.
High-Flux Design: Intended for suitable high-flux haemodialysis treatments.
Semipermeable Membrane: Allows prescribed solute and fluid transport.
Maximum Transmembrane Pressure: 600mmHg, according to the device registration.
Latex-Free: Manufacturer declares no latex content.
DEHP-Free: Manufacturer declares no DEHP content.
Gamma Sterilized: Supplied sterile.
Single-Use: Not intended for reuse.
Storage Temperature: 0°C to 30°C.
Professional Renal Care Application: Intended for appropriate haemodialysis treatment.
The Diacap Pro19H Dialyzer price in Kenya depends on manufacturer reference, membrane specifications, procurement quantity, packaging configuration and availability.
Healthcare facilities should confirm that their quotation identifies the exact B. Braun Diacap Pro19H, reference 720DH19G, rather than another membrane surface area or low-flux variant.
Manufacturer and Brand
The product is manufactured by B. Braun as part of the Diacap Pro renal care range.
Membrane Surface Area
The Pro19H has a membrane surface area of 1.9m².
High-Flux Membrane Classification
High-flux and low-flux dialyzers have different membrane characteristics and clinical applications.
Membrane Material
The product uses a polysulfone hollow-fibre membrane.
Manufacturer Reference
The specified product reference is 720DH19G.
Packaging Quantity
The number of dialyzers required affects institutional procurement.
Sterile Packaging and Shelf Life
Original packaging, batch information and sufficient remaining shelf life are important considerations.
Product Availability
Availability depends on current stock and supply arrangements.
Order Online: Maesio Pharmaceuticals Online Shop
The B. Braun Diacap Pro19H is intended for healthcare facilities providing prescribed haemodialysis treatment using suitable equipment and bloodline systems.
Its high-flux membrane characteristics and 1.9m² surface area provide a defined technical configuration for renal care procurement.
Hospital renal units.
Haemodialysis centres.
Specialist kidney care clinics.
Nephrology departments.
Renal replacement therapy facilities.
Hospital dialysis departments.
Specialist renal care centres.
Healthcare facilities providing maintenance haemodialysis.
Hospital procurement and biomedical departments.
Provides the semipermeable membrane used for blood purification during prescribed haemodialysis treatment.
Supports diffusion of suitable dissolved substances across the dialysis membrane.
Allows controlled ultrafiltration when operated with compatible dialysis equipment under the prescribed treatment conditions.
The membrane is designed for relatively high hydraulic permeability.
Supports prescribed solute exchange between blood and dialysate.
Forms the filtration component of a compatible haemodialysis circuit.
The Diacap Pro19H contains a bundle of hollow fibres made from a semipermeable polysulfone membrane.
During suitable haemodialysis treatment, blood circulates through the blood compartment of the dialyzer.
Dialysis fluid flows through the separate dialysate compartment.
The membrane separates these two fluid pathways while permitting selected transport processes.
Small dissolved substances can move across the membrane according to their concentration gradients.
The dialysis machine controls fluid removal by regulating the relevant treatment pressures and parameters.
When fluid crosses the membrane, dissolved substances may be transported with the fluid according to the membrane properties and prescribed treatment conditions.
The performance of these processes depends on the complete dialysis system.
The dialyzer does not operate independently and cannot replace the dialysis machine, bloodlines or appropriate vascular access equipment.
The 1.9m² designation describes the effective membrane surface area specified for the Pro19H.
Surface area is an important dialyzer-selection parameter.
However, a larger membrane surface area does not automatically produce better clinical outcomes for every patient.
The treating nephrologist must consider patient characteristics, dialysis prescription, clearance requirements and extracorporeal circuit volume.
High-flux dialyzers have membrane characteristics that permit comparatively greater water movement under appropriate pressure conditions than conventional low-flux membranes.
These characteristics may also support the clearance of selected middle-molecular-weight substances.
However, high-flux design does not mean that every substance will be removed effectively or that every treatment should use the same dialyzer.
Appropriate selection depends on the prescribed treatment.
Membrane characteristics.
Membrane surface area.
Prescribed blood flow.
Dialysate flow.
Treatment duration.
Ultrafiltration conditions.
Patient-specific characteristics.
Vascular access performance.
Circuit and machine compatibility.
Can be selected for prescribed haemodialysis treatment when its membrane properties and dimensions are appropriate.
May be used in compatible extracorporeal renal replacement systems.
Designed for treatments requiring a suitable high-flux membrane.
Provides a defined dialyzer configuration for professional renal treatment.
Suitable for healthcare facilities ordering the specified single-use dialyzer.
These products have different membrane surface areas and blood compartment volumes.
The same membrane surface area does not mean that two dialyzers have identical membrane permeability or treatment performance.
These are complementary categories of dialysis consumables, not equivalent products.
Designed for prescribed treatments requiring high-flux membrane characteristics.
Provides a clearly specified membrane area for clinical selection.
Uses B. Braun's specified high-flux membrane material.
The 120mL blood compartment volume supports accurate assessment of extracorporeal circuit requirements.
B. Braun confirms these material declarations.
The product is supplied sterile.
Designed for one treatment rather than repeated patient use.
Store the unopened Diacap Pro19H within the manufacturer's specified temperature range of 0°C to 30°C.
Keep the dialyzer in its original packaging until required.
Protect it from physical damage and unsuitable environmental conditions.
Verify the model and manufacturer reference.
Inspect the sterile packaging before use.
Check the expiry date and batch number.
Do not use the dialyzer if the sterile barrier is damaged.
Follow the manufacturer's approved preparation and priming instructions.
Do not reuse or resterilize the product.
Dispose of used dialyzers according to appropriate blood-contaminated healthcare waste procedures.
The Diacap Pro19H is a professional medical device intended for use under appropriate clinical supervision.
Its selection must be based on the patient's dialysis prescription and relevant clinical characteristics.
The 120mL blood-side priming volume should be considered as part of the extracorporeal circuit assessment.
The dialyzer's maximum transmembrane pressure of 600mmHg must not be interpreted as a recommended treatment setting.
The treating team must follow the manufacturer's operating limits and the dialysis machine's approved procedures.
Potential complications associated with extracorporeal dialysis include blood loss, clotting, haemolysis, adverse membrane reactions and fluid or electrolyte disturbances.
Correct machine setup, monitoring and clinical assessment remain essential.
The Diacap Pro19H is single-use and should not be reprocessed for another treatment.
What is Diacap Pro19H Dialyzer?
It is a sterile B. Braun high-flux hollow-fibre haemodialysis dialyzer with a 1.9m² polysulfone membrane.
What is the Diacap Pro19H Dialyzer price in Kenya?
The price depends on product availability, procurement quantity and packaging requirements.
Where can I buy Diacap Pro19H in Nairobi?
You can order or enquire through Maesio Pharmaceuticals Limited.
Who manufactures Diacap Pro19H?
The product is manufactured by B. Braun.
What is the manufacturer reference?
The exact listed reference is 720DH19G.
Is Diacap Pro19H a high-flux dialyzer?
Yes. B. Braun identifies it as a high-flux dialyzer.
What is the membrane surface area?
The membrane surface area is 1.9m².
What membrane material is used?
The dialyzer uses a polysulfone membrane.
What is the blood-side priming volume?
The blood compartment volume is 120mL.
What is the housing material?
B. Braun specifies polycarbonate.
What does the H in Pro19H mean?
It identifies the high-flux version within the Diacap Pro range.
What is the difference between Pro19H and Pro19L?
Pro19H is high-flux, while Pro19L is low-flux.
What is the difference between Pro19H and Pro16H?
Pro19H has a 1.9m² membrane area, while Pro16H has a 1.6m² membrane area.
What is the difference between Pro19H and Pro13H?
Pro19H has a 1.9m² membrane area, while Pro13H has a 1.3m² membrane area.
What is the maximum transmembrane pressure?
The registered device specification lists 600mmHg as the maximum TMP, not a recommended operating target.
Can the dialyzer remove urea?
Yes. The semipermeable membrane supports prescribed urea clearance during suitable dialysis treatment.
Can it remove excess fluid?
Yes. Controlled ultrafiltration can occur under the prescribed dialysis conditions.
Can it be used for every dialysis patient?
No. Dialyzer selection depends on the patient's clinical requirements and treatment prescription.
Does the dialyzer contain latex?
B. Braun declares that the product does not contain latex.
Does it contain DEHP?
No. B. Braun declares no DEHP content.
Is the Diacap Pro19H sterile?
Yes. It is supplied sterile.
How is the dialyzer sterilized?
B. Braun specifies gamma sterilization.
Can it be reused?
No. It is a single-use dialyzer.
What is the storage temperature?
B. Braun specifies 0°C to 30°C.
Is it compatible with all dialysis machines?
No. Equipment and bloodline compatibility must be verified.
Can it be used with DiaStream Classic HDF?
A suitable bloodline set may be selected, but compatibility must be confirmed for the complete treatment system.
Is DiaStream Classic HDF a dialyzer?
No. It is a bloodline system, while Diacap Pro19H is the filtration device.
Does the product include fistula needles?
Fistula needles are separate dialysis vascular access products unless specifically included in a confirmed procurement package.
Can dialysis centres order several units?
Yes. Institutional quotations can be requested according to facility requirements.
What should I confirm before ordering?
Confirm reference 720DH19G, high-flux classification, 1.9m² membrane area, sterile packaging, expiry date and required quantity.
Does Maesio Pharmaceuticals arrange delivery outside Nairobi?
Yes. Delivery to other locations in Kenya can be discussed according to product availability and order requirements.
Technical Specification Note: The verified B. Braun Diacap Pro19H, reference 720DH19G, is a high-flux hollow-fibre dialyzer featuring a 1.9m² polysulfone membrane, 120mL blood-side priming volume and polycarbonate housing. It is sterile, gamma-sterilized, latex-free, DEHP-free and single-use.
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The Diacap Pro19H Dialyzer is a sterile B. Braun high-flux haemodialysis dialyzer designed for professional renal replacement therapy.
Its 1.9m² membrane surface area, polysulfone hollow-fibre construction and 120mL blood-side priming volume provide a clearly specified configuration for hospital and dialysis centre procurement.
The product is intended for use with compatible haemodialysis equipment and prescribed extracorporeal treatment systems.
Before purchasing, healthcare facilities should confirm the exact manufacturer reference, membrane surface area, sterile packaging, expiry date and required order quantity.
Maesio Pharmaceuticals Limited supplies B. Braun Diacap Pro dialyzers, dialysis bloodline systems, fistula needles, dialysis machine cleaning products and related renal care consumables for healthcare facilities across Kenya.
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