Put to the test: Challenges in catheter testing

Manufacturers of catheter systems develop standard and custom catheters, stents, and guide-wires to meet surgical needs. ZwickRoell highlights some of the catheter testing challenges it meets using its expertise.

Increasing regulatory pressure is challenging medical equipment manufacturers to meet strict requirements in design, testing, and production. This trend is reflected in catheter systems that are used for vascular surgery along with coronary stents.

There are many types of catheters including those used to transport small instruments or repair devices to a particular site in the body. Some catheters have small built-in tools so that a surgeon can repair a problem in the patient’s body without having to perform open heart surgery, while some can deploy a stent that will keep an artery open.

For surgeons, challenges associated with such procedures include feeding catheters into femoral arteries, navigating sharp turns, and advancing the device without damaging tissue. Manufacturers of catheter systems work closely with surgeons to develop standard and custom catheters, stents, and guide-wires to meet these challenges.

Catheter manufacturers continually monitor their product by physically testing the complete units, as well as individually testing the component parts. To properly test such devices, catheter manufacturers need to replicate the condition of a patient lying on an operating table and a surgeon inserting a catheter.

‘Pull-off’ testing is important because joined parts should not fail when the catheter is inside the patient. Stents are tested, both in compression and flexure modes, and the frictional behaviour of the complete catheter is measured as it is pushed through a simulated artery known as a ‘tortuous path’.

To facilitate this action, ZwickRoell has developed a system that controls the test machine crosshead and special automated pneumatic grips. The horizontal machine is essentially a test bed that incorporates space above and below the main test axis to accommodate 3-D models and water baths.

In a typical test, the testing machine pushes the catheter into the tortuous path for a designated distance before the pneumatic grip then releases the catheter and the crosshead moves back to the original start point. The pneumatic grips close onto the catheter, moving the crosshead forward once again.

This sequence is repeated until the catheter has been fully inserted into the simulated artery. This test procedure, which is fully automated, can easily accommodate different sizes of tortuous paths and the machine software enables the following results to be calculated:

Track force, push efficiency, insertion force measurement, guide-wire movement, flexibility, guide-wire and catheter lubricity track measurement.

The results can be calculated with high precision. The extremely stiff load frame with digital control and drive systems ensures that forces measured during the test originate from the sample under test and not from within the machine itself.

The machine control system has such a high degree of accuracy and resolution that it can position the crosshead of the machine to less than 1 µm, and read forces to an accuracy of better than 0.5 % down to values of less than 0.1 mN.

The machine software platform can control all of the test parameters including the safety features of the testing machine. At the same time, it can acquire and process the raw test data in real-time and store this data, as individual data points and as calculated result data.

Stringent regulatory environments require the ability to maintain accurate records of the testing procedures and results. Record keeping requirements are described under FDA 21 CFR Part 11.

Part 11 requires drug makers and medical device manufacturers, biotech companies and other FDA-regulated industries to implement controls, including audits, system validations, audit trails, electronic signatures, and documentation for software and systems involved in processing electronic data that are required to be maintained by FDA predicate rules or used to demonstrate compliance to a predicate rule.

Record keeping to satisfy Part 11 standards, can be integrated as an option into software. Medical device companies can take full advantage of this feature and save the costs of third party accreditation.

The software includes the functions; “Electronic Records and Signatures” for complete digital documentation of all safety critical tests. Test results can be automatically stored in the customer’s database.

Operator and environment safety concerns are also critical. The testing equipment can be supplied with splash-proof electrical connectors and a supplementary emergency stop button for additional safety.

A software plug-in is available that enables a standard video camera to be connected to the system to record the test sequence. The incoming video signal is automatically synchronised with the force and displacement data. It allows a more complete record of the test to be saved or transmitted to interested third parties.