Efficient Pulsed Vacuum Steam Sterilizer for Surgical Tools with Hinged Door Access

Yes, we are a professional manufacturer of pharmaceutical and laboratory sterilizers, integrating R&D, production, and international trade. We warmly welcome on-site factory visits and remote video factory inspections, so you can verify our production capacity and quality control system.

Yes. Our sterilizers are designed and manufactured following GMP guidelines, FDA 21 CFR Part 11 (electronic records & signatures), and other global pharmaceutical regulatory requirements. They are fully suitable for use in GMP-compliant production environments in pharmaceutical factories and laboratories.

Absolutely. We provide complete, audit-ready documentation packages in accordance with pharmaceutical industry practices and GAMP 5 guidelines, including but not limited to design documents, validation documents, SOPs, FAT, SAT, IQ/OQ/PQ, material certificates, calibration records, and other supporting documents. This documentation fully supports your regulatory audits for pharmaceutical and laboratory applications.

The equipment uses saturated steam as the sterilizing medium. Through repeated vacuum-pumping and steam-injection cycles, residual air within the chamber and loads is efficiently eliminated to optimize steam contact and penetration.

The MQA series can be supplied in single-door or pass-through double-door versions to meet diverse requirements for sterilization capacity and isolation management.