Service Swiss Medtech Expo 2023

The only one of its kind in the world: Validated packaging process from a single source

We offer you a complete packaging process: Our qualified packaging machine, which documents all processes and provides validated packaging material with a shelf life of up to 10 years.

  • Medical device packaged with the VC999® C6 Medical vacuum chamber machine
    Medical device packaged with the VC999® C6 Medical vacuum chamber machine
  • Possible medical devices that the VC999® C6 Medical Vacuum Chamber Machine packages
    Possible medical devices that the VC999® C6 Medical Vacuum Chamber Machine packages
  • Medical devices packaged with the VC999® C6 Medical vacuum chamber machine
    Medical devices packaged with the VC999® C6 Medical vacuum chamber machine
  • Medical device packaged with the VC999® C6 Medical vacuum chamber machine
    Medical device packaged with the VC999® C6 Medical vacuum chamber machine

Our worldwide unique offer

Together with our own packaging validation for Tyvek®, vacuumable PAPE and paper/film bags with a shelf life of up to 10 years, we offer you a complete packaging process that is unique in the world, without you having to carry out time-consuming and costly packaging validation yourself. We also offer you a strong alliance with our international partners.

Your benefits at a glance

  • High speed machine with up to 40 pieces vacuuming and sealing / 1 min.
  • Permanently heated sealing bars, with tightest tolerances
  • External pump, reduces noise and oil changes in your clean room
  • 100% real-time recording of processing data (audit trail)
  • Barcode scanning
  • "All in One" machine for almost any application for long, high and heavy as well as small and light pieces

+ Pre-validated bags with a shelf life up to 10 years, no need for customer's own aging study for packaging validation, saving time and cost

+ available for materials: PA/PE (vacuumable), Tyvek®, paper/film.

 

ISO certification

Our packaging process meets the stringent requirements of MDR, GMP and ASTM standards. Confirmed during an EN ISO 13485:2016 audit.

 

 

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