MIZ-MA LLC is committed to quality, safety, and compliance with the highest international and national standards. All our products undergo rigorous quality control at every stage of production, as confirmed by the relevant certificates and declarations.
ISO 13485 Certificate
Our production is certified under the international ISO 13485 standard, which sets requirements for a quality management system for medical device manufacturers. This certification ensures that all processes—from development to product release—meet the highest safety, reliability, and efficiency standards.
Compliance with the Ministry of Health of Ukraine Requirements
All MIZ-MA products comply with the current regulatory requirements of the Ministry of Health of Ukraine, as confirmed by the necessary certificates and declarations. We ensure that our products fully meet safety and performance standards required for use in medical institutions.
Compliance with the Technical Regulations for Medical Devices
The equipment and furniture manufactured by MIZ-MA comply with the technical regulations for medical devices, as confirmed by certificates of conformity and declarations of conformity.
This category includes:
• Air sterilizers
• Steam sterilizers
• Paraformaldehyde chambers
• Dry-air thermostats
• Dry-air thermostats with cooling
• Medical furniture
These documents confirm that our products meet all necessary technical, operational, and safety requirements, making them suitable for use in medical institutions.
Quality and Safety Guarantee
We are committed to providing our customers with certified medical equipment that meets all legal requirements. By choosing MIZ-MA, you receive products that have undergone thorough testing, are backed by the necessary documentation, and comply with all modern standards in the medical device industry.