Medical Devices
Tunix Corporation: Precision Environmental Test Chamber for Medical Devices
At Tunix Corporation, we deliver confidence to the healthcare technology sector by providing advanced environmental testing solutions engineered for precision, compliance, and patient safety. From surgical instruments to implantable electronics, our test chambers simulate real-world conditions to validate performance, durability, and regulatory readiness—because in healthcare, failure is not an option.
Meeting Global Standards. Ensuring Life-Saving Reliability.
Our test chambers for medical devices are built to exceed the industry’s most demanding standards, ensuring absolute consistency and traceability in your quality assurance process.
- ISO 13485 – Support for medical device quality management systems
- IEC 60601 / IEC 61010 – Environmental validation for electrical medical equipment
- FDA / EU MDR Guidelines – Aligned with global regulatory pathways for market entry
- GMP Compliant Protocols – Designed for validation and clean manufacturing environments
Medical Devices Tested in Tunix Chambers
| Test Category | Devices & Components Evaluated |
| Thermal Cycling | Syringes, catheters, tubing, housings, enclosures |
| Humidity / Condensation | Electronic monitors, wearable sensors, adhesives, coatings |
| Accelerated Aging | Packaging, IV bags, wound dressings, implant coatings |
| Ingress (Dust/Water) | Infusion pumps, patient monitors, surgical instruments |
| UV / Light Exposure | Transparent packaging, light-cured adhesives, optics |
| Vibration / Shock | Diagnostic equipment, mobile health units, pacemaker components |
| Cold / Heat Storage | Vaccines, blood storage containers, temperature-sensitive devices |
Tunix Corporation: Enabling Safe Innovation in Healthcare
Your medical devices are designed to save lives—we’re here to ensure they can stand up to the environments in which they’re used. Tunix test chambers provide the precision, repeatability, and compliance needed to move your product confidently from R&D to regulatory approval and into the hands of clinicians worldwide.
