Renatron Reprocessing System Application: Dialyzer Reprocessin

The Renatron II 100 Series Dialyzer Reprocessing System is indicated for the in vitro rinsing, cleaning, testing, and delivery of proportioned Cold Sterilant solution to hollow fiber dialyzers.


It is also indicated for record keeping of these functions.

The Renatron II Dialyzer Reprocessing System automatically reprocesses dialyzers used by kidney dialysis patients and provides valuable data for record keeping and quality control.

Since the introduction of RenatronAR, hundreds of millions of dialyzers have been processed. The current Renatron model, the RenatronAR II 100 Series brings all of the best features of the original, but includes critical enhancements determined by our customers.



Health & Safety standards

A. Compliance with USA FDA protocols/ guidelines

A. NSAI Quality System Approval certificate

A. Validated for JCI/ NABH Accredition

A. AAMI/ ANSI Guidelines followed

A. Quality assurance for Hemodialyzer Reprocessing articles on Renatron II 100 / Renalin 100

A. National Kidney Foundation Council on use of Reprocessing System

A. As per Safe Medical Devices Act of 1990 FDA Publication (FDA 91-4243)

A. Guidelines as per HCFA (Health Care Financing Administration)

Key Features

A. Automated reprocessing cycle: 8-10 minute cycle flushes, cleans, tests and fills dialyzers automatically

A. Venous line clamp

1. Prevent cross contamination

2. Secure Venous outlet line

A. Colour coding: Provide visual cues to dialyzer orientation

A. More defined control panel areas

A. Header Integrity test: Diagnostic test to verify that the header is on securely with a Oa ring in place

A. Failed Volume test: Limiting the number of retests to 2 to get more accurate counts

A. Culture sample cycle: Separate cycle for ease of taking water samples

A. Dedicated clean/rinse cycle: Aggressive Formula 409A cycle for heavily deposited lines and machines