Why Buy Van der Stähl?
There are a host of reasons to buy your critical packaging machinery from Van der Stähl Scientific, from state-of-the-art technology to our world-class customer support. The differences count.   learn more

Power to Control
Center to package validation is managing critical control attributes of the sealing process

The MD-850 medical pouch sealer's microprocessor allows quality teams to set up the machinery utilizing the simple step menus. The microprocessor also allows for the management of the printing functions to be setup and controlled on the controller's menu system.

Validation Report Radio
This year, we will bring you updated news on the sterile barrier system broadcasted right to you

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Packaging Resources
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Read About our Industry
Learn about shifting trends in the medical device manufacturing and medical device packaging industry with news from our on-staff and adjunct writers.     learn more

This sealer represents years of development and utilizes the most advanced technology for the sealing of terminally sterile flexible packs. Continuous Film Sealing Machine MD-850 with integrated, microprocessor controlled printing unit. Optimum sealing safety for packing sterile goods e.g. in clinics and laboratory environments. Under the new sterile barrier system, medical device packagers will be asked to evaluate not only seal strength but seal integrity. That has put higher demands on the machinery utilized for the process of packaging terminally sterile goods.

The MD-850-US medical pouch sealer represents the most advanced microprocessor-controlled packaging offered in the medical device arena, with finely tuned pressure transducers and thermal probes with high accuracy and acuity. The MD-850 medical device sealer is an excellent choice for packaging your sterile product against this new robust standard.

The sterilization of medical instruments begins with the packaging. That is to say that the packaging, and therefore also the validation of the packaging process, is crucial for guaranteeing sterility up to the point of use and for meeting quality standards.

The ISO 11607 standard demands explicitly reproducible processes in order to achieve optimum and constant results at all times during Operation Qualification. The critical process parameters must be monitored continuously. If there is any deviation, the device must immediately switch itself off and indicate what the problem is. The sealing of a sterile package is only possible with a sealing device that can be validated in accordance with ISO 11607.

The MD-850-US is the ideal sealer for the packaging of sterile goods in clinics and laboratories, satisfying the highest quality and safety standards. Call and speak with a validation engineer. We will be glad to generate a pouch study with your pouches to determine machine settings to generate compliant seals.

Superb German engineering delivers accurate seal to seal consistency. Backed by Van der Stähl Scientific's world class validation support program. Remember NIST traceable calibration, free preventative maintenance software, free package integrity studies in our comprehensive pack lab and toll free validation support from our on-staff CPP. Contact technical support or customer service now toll free at 1-800-550-3854.