At Ceres Testing, our mission is to provide accurate and reliable testing services to our clients. We are committed to upholding the highest standards of quality and integrity in every test we conduct.
Our team of expert testers will ensure that your product meets all quality standards and requirements before launch.
We offer comprehensive list of tests outlined in ISO 10555-1 providing general requirements for testing intravascular catheters, ensuring they meet safety and performance standards. Below is a brief summary of the different testing's offered:
Dimensional Testing: Verifies catheter dimensions like diameter and length to ensure consistency with specifications.
Tensile Strength Testing: Assesses the catheter’s resistance to breaking under tension, ensuring durability during use.
Flexural Resistance: Evaluates the catheter’s flexibility and ability to withstand bending forces without damage.
Flow Rate Testing: Measures the fluid flow rate through the catheter to confirm proper performance for medical applications.
Kink Resistance: Determines the catheter’s ability to resist kinking, which could impede fluid delivery.
Liquid Leak Testing: Checks for any leakage under pressure to verify product integrity and patient safety.
Hub Air Leak Testing: Checks for air leaks under vacuum to verify product integrity and patient safety.
Corrosion Resistance: Ensures materials used in the catheter can withstand exposure to fluids without degradation.
These tests are crucial for manufacturers to ensure compliance with regulatory requirements and provide safe, high-quality medical devices.
We offer comprehensive list of tests outlined in ISO 25539 - Part 1 providing the testing requirements for endovascular medical devices, such as stents and grafts, to ensure safety and performance. Below is a brief summary of the different testing's offered:
Dimensional Verification: Confirms device measurements, including diameter and length, to meet specifications.
Radial Force Testing: Evaluates the outward force exerted by the device to ensure adequate vessel support.
Flexibility and Kink Resistance: Examines the device's ability to bend and conform without damage.
Coating Integrity: Ensures that any surface coating remains intact during handling and deployment.
Crimping and Expansion Testing: Verifies proper functionality during crimping onto a delivery system and expansion within a vessel.
Delivery, Deployment and Retrieval Force Testing: Tests the amount of force required to delivery, deploy and retrieve the implants.
These tests are crucial for manufacturers to ensure compliance with regulatory requirements and provide safe, high-quality medical devices.
We offer particulate testing in compliance to USP 788, the standard for particulate testing in injectable medical devices to ensure they meet safety and quality requirements. This testing evaluates the presence of subvisible particles, which could pose risks to patients if introduced into the body. We offer both methodologies outlines in the standard that is light obscuration and microscopic particle counting to quantify particulate levels. Compliance with USP 788 is essential for manufacturers to ensure product reliability and meet regulatory requirements.
We conduct thorough usability testing to ensure that your product is user-friendly and easy to navigate.
We test your product's compatibility with different devices and platforms to ensure that it works seamlessly across all compatible devices.
We love our customers, so feel free to visit during normal business hours.
1 Technology Drive, Suite B 107,Irvine, CA 92618, USA
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