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Your turn-key packaging solution

Time is money – efficient and cost saving packing-solutions by puracon

You not only benefit from our extensive experience and know-how, but also from short processing times and prevalidated packaging solutions that give you the opportunity to extend the shelf-life of your products up to seven years.

Cleaning, assembly and packaging of sterile products is done exclusively in our GMP qualified class C cleanroom. For products with particularly high demands on environmental conditions, we have laminar-airflow boxes of GMP class A available.

puracon is certified according to ISO 13485, registered with the FDA and accredited in Japan. Experience our premium services and benefit from our extensive experience and know-how, combined with highest quality and efficiency standards.

Quality and safety first – 5 steps towards a successful sterile packaging concept

Listening to our customers is one of our top priorities as this ensures full understanding of your needs and expectations in terms of timing, costs, volumes and the packaging concept that is best for your product. Our puracon 5 steps packaging process helps you making the right choices and provides you with all you need to define the perfect solution within your individual requirements.

 

Pre-validated medical device packaging concepts

Our pre-validated sterile medical packaging concepts are the right solution for you, if your objective is a fast and standardized ready-to-market solution at low investment costs.

Our concept of prevalidated seal shapes provides a variety of different blisters, shapes and sizes that can be easily combined. Our broad portfolio of pouches in different materials, sizes and shapes covers further alternatives for prevalidated packaging concepts. All solutions are available with a shelf-life up to seven years.

What if you need a non-prevalidated but customized solution? Our service does not only cover prevalidated packaging concepts, but also extends to packaging design, validation consulting, organizing those validations and consulting on product approvals.