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Parjet Has Achieved ISO 13485 Certification

Parjet has successfully achieved ISO 13485 certification for Medical Device Quality Management Systems, demonstrating that our quality management, process control, and risk management capabilities fully comply with international medical device requirements.

ISO 13485 is a key quality standard within the medical device supply chain, with a strong focus on product consistency, traceability, and risk control. This certification confirms that Parjet’s sealing manufacturing processes are capable of supporting the stability and reliability required for medical applications.

With ISO 13485 certification, Parjet is able to better support medical device manufacturers in meeting regulatory requirements, reducing supply chain risks, and delivering sealing solutions suitable for critical medical fluid, gas, and system applications.

Medical-Grade Manufacturing and Quality Control
Medical-grade manufacturing ensures consistent and reliable sealing performance.

Full Traceability and Controlled Change Management
Materials, processes, and batches are fully traceable with controlled change management.

Support for Medical Regulatory and Production Requirements
Reliable support for medical regulatory compliance and mass production.

Parjet will continue to strengthen its quality management system and leverage medical-grade sealing technologies to become a trusted partner for customers in medical device applications.