Your advantages as a stericlin® customer
Responsibility results in commitment - for more than 45 years
For more than 45 years we produce, under the brand name stericlin®, indicator systems, sterile barrier systems and sterilisation accessories. Our customers include hospitals, doctors' offices and service providers in Germany and more than 70 other countries.
Quality and safety
Our products are manufactured in modern production plants under clean room conditions and on the basis of carefully validated production processes. These include around the clock in-process controls and complete IT-based traceability of all materials used. As a stericlin® customer, you can always rely on the quality of our products.
Requirements to meet the standard
The requirements of national and international standards and laws for medical devices form the basis for the development and manufacturing of our products. These are the DIN EN ISO 11140-4 and 11140-3 for Bowie-Dick test systems, the DIN EN 867-5 for batch monitoring systems and DIN EN ISO 11607 and DIN EN 868 for sterile barrier systems. Our cleanroom classified ISO 8 according to DIN EN ISO 14644 part 1 and 3 is ISO 13485 certified. In addition, we let our products be checked externally for the compliance with the strict standard requirements. For example, our Bowie-Dick single use test pack has obtained the Kitemark of the British Standards Institution (BSI), a prestigious and internationally recognised test institute.
Service and support
For us, outstanding service and satisfied customers are in the centre of our business. Increased demands placed on your staff in the CSSD’s and specialised departments require constant training. We support you! You receive detailed training on site by our knowledgeable staff in theory and practice on the proper handling of sterile barrier systems, sterilisation accessories and indicator systems.
Our wide range includes indicator systems, sterile barrier systems, sterilisation equipment, products for labelling and documentation, products for sterile goods logistics and hygiene. Our aim is to continually develop our products based on your requirements and the applicable standards and regulations for medical devices. When new products originate in this way, our security bags for disinfected medical devices as a concept are based on the 2015 recommendation of the DGSV’s Quality Task Group (90).
Our high storage capacity and state-of-the-art storage technology guarantee safe loading and short-term delivery to you. We maintain a complete system of connected processes, whose optimisation leads to a reduction of processing and response times.
Environmental awareness is in our part of the company policy: we work 100% climate neutral. Unavoidable emissions are fully offset through internationally recognised emission reduction certificates. In addition, we meet all the requirements of DIN EN ISO 14001 in environmental management and ISO 50001 for energy management.