MEDICAL
PACKAGING
MV provides a wide range of medical packaging formats in different materials, suitable for several medical devices intended to ETO sterilisation.
Why it’s important
Primary medical packaging is a critical process in manufacturing single use medical devices because it has to: ensure sterility of the device for a certain period of time, open without releasing particulates and avoid contamination of the packaging materials on the devices.
MV has gained years of experience in the sector of medical packaging, now offering a top quality service using validated highest standard packagin machines, certified and verified suppliers of materials and ongoing controls on sealing, materials and packaing itself. With 7 packaging machines in our ISO 7 Clean Room we offer more than 30 different formats for packaging of medical devices.
Our formats
From the largest 300×210 mm format to the smallest 37×60 mm format, we offer a complete range of formats, suitable for every type of single use medical device. Customization on client request is always possible and our Technical Office is available for design and development of new formats, either in soft or stiff plastic film.
Materials
The choice of packaging material is very important and critical to allow the highest quality standard we offer. Materials used for medical packaging are: medical paper and plastic medical film.
Services
STERILIZATION
MV offers several services for clients and partners, from working processes such as tube cutting, assembly and device testing, to the support for certification and distribution of medical devices and to ETO sterilization.
ASSEMBLY AND TESTING
MV offers several process support to its clients such as tube cutting, assembly and bonding of components and kit, and testing od devices or lines. All the operations are conducted in ISO 7 clean room, a protect and monitored environment that minimizes contamination risk.
REGULATORY SUPPPORT
In the medical device sector the regulatory compliance is essential and we have always believed in it. We provide support to our clients who has neither resources nor structure to fulfill to strict regulatory requirements, registering our trade mark on specific devices or signing OBL contract. MV has obtained CE mark on 10 families of products, quality management system certification UNI EN ISO 13485:2016 and FDA 510k on one product distributed in the US.