Ensuring Excellence in Medical Product Development with SESS Test Chambers
Medical devices and products demand rigorous testing to ensure they meet international safety and performance standards. Sri Easwari Scientific Solution Pvt Ltd (SESS) provides state-of-the-art test chambers tailored to support the development, testing, and validation of medical products, ensuring compliance with global regulations.
How SESS Test Chambers Aid Medical Product Development
1. Temperature and Humidity Testing
- Simulates real-world environmental conditions to validate device performance across diverse climates.
Applications: Storage stability for drugs, vaccine temperature monitoring, and medical device durability tests.
2. Sterilization and Aging Testing
- Supports sterilization process validation through controlled temperature and humidity conditions.
- Accelerated aging chambers help predict product shelf life.
Applications: Disposable medical devices, surgical instruments, and packaging validation.
3. Corrosion Resistance Testing
- Ensures metallic components of devices withstand exposure to sterilization chemicals and bodily fluids.
Applications: Implants, surgical tools, and diagnostic equipment.
4. Environmental Simulation for Electronics
- Ensures reliability of electronics under extreme thermal and humid conditions.
Applications: Ventilators, infusion pumps, and monitoring systems.
5. IP Testing (Ingress Protection)
- Rain and dust test chambers verify device safety against water and particulate ingress.
Applications: Portable medical devices, wearable sensors, and home diagnostic tools.
6. Vibration and Shock Testing
- Combined chambers simulate vibrations and shocks experienced during transport.
Applications: Medical imaging devices, diagnostic machines, and sensitive equipment.
International Standards Covered by SESS Test Chambers
SESS chambers help manufacturers achieve compliance with key international standards:
1. ISO 13485 – Quality management system for medical devices.
2. IEC 60601 – Electrical safety standards for medical equipment.
3. ISO 11607 – Validation of medical device packaging.
4. USP <1079> – Storage and distribution of pharmaceuticals.
5. ISO 10993 – Biological evaluation of medical devices (biocompatibility).
6. ISO 14971 – Risk management for medical devices.
7. EN 60601-1-11 – Requirements for home healthcare devices.
Why Choose SESS for Medical Testing Needs?
1. Custom Solutions: Test chambers tailored to specific medical device requirements.
2. Compliance-Driven Designs: Aligned with international regulatory standards.
3. Advanced Features: Siemens PLC-controlled systems, data logging, and remote monitoring.
4. Energy Efficiency: Cost-effective and sustainable designs.
Partner with SESS for Safer, Smarter Medical Devices
Accelerate your product development journey with precision environmental testing. Explore our solutions tailored for the medical industry.
📧 info@sess.co.in | 🌐 http://www.sess.co.in

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