Dialyser

The Jindal Enterprises Dialyser is a hemodialysis machine designed for the removal of uremic toxins and excess fluid from the blood of patients with renal failure. The unit operates with a maximum blood flow rate of 300 mL/min and a dialysate flow rate of 500 mL/min. It includes integrated pressure sensors, air bubble detection, and conductivity monitoring for dialysate composition. The control panel features a touchscreen interface with multilingual support and alarm logs stored locally.

The dialyser uses hollow fiber membranes with a surface area of 1.8 m² to 2.2 m², made from polysulfone or polyethersulfone, both known for high biocompatibility and low protein adsorption. The membrane pore size is standardized at 2-3 nanometers to permit clearance of urea and creatinine while retaining albumin. The device supports single-use, disposable dialyzers and is compatible with standard dialyzer models conforming to ISO 8600-1. No reusable dialyser function is supported.

This device is used in hospital nephrology units, standalone dialysis centers, and home healthcare programs in regions with limited infrastructure. Buyers include public hospitals, private clinics, and NGOs supplying dialysis services. Units are typically sold individually, with bulk orders for 5+ units accepted. Packaging includes a protective plastic shroud, foam-lined crate, and English-language user manual. Lead time is 15 to 20 business days after order confirmation. Payment terms are negotiable, but the supplier does not specify Incoterms on the listing.

Jindal Enterprises is located at 13b, Mirza Ghalib Street, Kolkata, West Bengal, India. The company is registered as an importer and distributor of medical devices, with a harbor trust tier indicating verified business registration. The listing does not state whether the company manufactures the dialysers or sources them from another producer. No information is provided on staff size, years in operation, or clinical testing history.

The supplier does not list certifications such as ISO 13485, CE, or FDA clearance on the product page. There is no public data on product testing, clinical validation, or quality control procedures. Buyers must request copies of the CE mark, test reports, and import licenses directly. The supplier has no recorded response rate or communication history on the platform.